Wednesday, 11 July 2012

Albumin (Human)




FULL PRESCRIBING INFORMATION

PACKAGE LABEL - PRINCIPAL DISPLAY PANEL




Indications and Usage for Albumin (Human)



Hypovolemia


Albumin (Human) 20% is indicated in the emergency treatment of hypovolemia with or without shock. Its effectiveness in reversing hypovolemia depends largely upon its ability to draw interstitial fluid into the circulation. It is most effective in patients who are well hydrated. When blood volume deficit is the result of hemorrhage, compatible red blood cells or whole blood should be administered as quickly as possible. [1, 2]


When hypovolemia is long standing and hypoalbuminemia exists accompanied by adequate hydration or edema, 20% - 25% albumin solutions should be used. [1 ]



Hypoalbuminemia


For subjects with hypoalbuminemia who are critically ill and/or are bleeding actively, Albumin (Human) 20% infusions may be indicated. [3 ] When albumin deficit is the result of excessive protein loss, the effect of administration of Albumin (Human) 20% will be temporary unless the underlying disorder is reversed.



Prevention of Central Volume Depletion after Paracentesis due to Cirrhotic Ascites (Treatment Adjunct)


Albumin (Human) 20% may be used to maintain cardiovascular function following the removal of large volumes of ascitic fluid after paracentesis due to cirrhotic ascites. [2 ]



Ovarian Hyperstimulation Syndrome (OHSS)


Albumin (Human) 20% may be used as a plasma expander in fluid management relating to severe forms of ovarian hyperstimulation syndrome (OHSS). [7, 8]



Adult Respiratory Distress Syndrome (ARDS) (Treatment Adjunct)


Albumin (Human) 20% infusions may be indicated in conjunction with diuretics to correct the fluid volume overload associated with ARDS. [5 ]



Acute Nephrosis (Treatment Adjunct)


Albumin (Human) 20% may be used to treat edema in patients with acute nephrosis who are refractory to cyclophosphamide and corticosteroid therapy. [1 ]



Hemolytic Disease of the Newborn (HDN)


Albumin (Human) 20% is indicated in the treatment of hyperbilirubinemia. It may be used prior to or during an exchange procedure in an attempt to bind free and to enhance its removal. [6 ]



Albumin (Human) Dosage and Administration



Dosage


General Recommendations


The concentration of the albumin preparation, dosage and the infusion rate should be adjusted to the patient’s individual requirements.


The dose required depends on the body weight of the patient, the severity of trauma or illness and on continuing fluid and protein losses. Measures of adequacy of circulating volume and not plasma albumin levels should be used to determine the dose required.


The daily dose should not exceed 2 g of Albumin (Human) 20% per kg of body weight.


Hypovolemia


In adults, an intravenous infusion of 25 g should be given. If adequate response (stabilization of circulation) is not achieved within 15 to 30 minutes, an additional dose may be given.


In spite of limited information about the efficacy in pediatric subjects, an intravenous infusion of 2.5 to 12.5 g or 0.5 to 1 g/kg body weight may be given. If adequate response (stabilization of circulation) is not achieved within 15 to 30 minutes, an additional dose may be given.


Hemodilution may follow administration of Albumin (Human) 20%. If hemorrhage has occurred, this may result in relative anemia. This condition should be controlled by the supplemental administration of compatible red blood cells or compatible whole blood.


Hypoalbuminemia


In adults, intravenous infusion of 50 to 75 g of Albumin (Human) 20% may be used. Hypoalbuminemia is usually accompanied by a hidden extravascular albumin deficiency of equal magnitude. This total body albumin deficit must be considered when determining the amount of albumin necessary to reverse the hypoalbuminemia.


In burns, therapy usually starts with the administration of large volumes of crystalloid injection to maintain plasma volume. After 24 hours, Albumin (Human) 20% may be added at an initial dose of 25 g with the dose adjusted thereafter to maintain a plasma protein concentration of 2.5 g per 100 mL or a serum protein concentration of 5.2 g/100 mL.


Prevention of Central Volume Depletion after Paracentesis due to Cirrhotic Ascites


In adults, intravenous infusion of 8 g of Albumin (Human) 20% may be given for every 1,000 mL of ascitic fluid removed.


Ovarian Hyperstimulation Syndrome


In adults, as a guideline, doses of 50 – 100 g of Albumin (Human) 20% should be infused over 4 hours and repeated at 4- to 12-hour intervals as necessary, when infusion of normal saline fails to achieve or maintain hemodynamic stability and urine output. [7 ]


Adult Respiratory Distress Syndrome (ARDS)


In adults, a dose of 25 g of Albumin (Human) 20% can be infused over 30 minutes and repeated at 8 hour intervals for 3 days, if necessary. [5 ]


Induction of Diuresis in Patients with Acute Nephrosis


In adults, a dose of 25 g of Albumin (Human) 20% can be infused, administered with an appropriate diuretic once a day for 7 to 10 days.


Hemolytic Disease of the Newborn


In newborns, Albumin (Human) 20% may be administered prior to or during exchange transfusion at a dose of 1 g per kilogram body weight. [6 ]



Administration


Intravenous use only.


Prior to administration, parenteral drug products should be inspected visually for turbidity and discoloration, whenever solution and container permit.


Do not dilute with sterile water for injection.


Do not use solutions of Albumin (Human) 20% which are cloudy or have deposits. Once the infusion container has been opened the contents should be used immediately. Discard the unused portion. Filtration of Albumin (Human) 20% is not required.


The infusion rate should be adjusted according to the individual circumstances and the indication. In plasma exchange during paracentesis, the infusion rate may be higher and should be adjusted to the rate of removal.


If large volumes (greater than 1500 ml) are administered, the product should be warmed to room temperature before use.



Dosage Forms and Strengths


Albumin (Human) 20% is supplied in


  • 10 g in 50 mL infusion bottle

  • 20 g in 100 mL infusion bottle

Do not use in individuals who are hypersensitive to albumin preparations, any ingredient in the formulation, or components of the container.



Warnings and Precautions



Hypersensitivity


Hypersensitivity or allergic reactions have been observed, and may in some cases progress to severe anaphylaxis. Epinephrine should be available immediately to treat any acute hypersensitivity reaction.



Hypervolemia/Hemodilution


Hypervolemia may occur if the dosage and rate of infusion are not adjusted to the patient’s volume status. At the first clinical signs of possible cardiovascular overload, e.g., headache, dyspnea, increased blood pressure, jugular venous distention, elevated central venous pressure, pulmonary edema, the infusion should be stopped immediately and the patient reevaluated. Albumin should be used with caution in conditions where hypervolemia and its consequences or hemodilution could represent a special risk for the patient. Examples of such conditions are:


  • Decompensated cardiac insufficiency

  • Hypertension

  • Esophageal varices

  • Pulmonary edema

  • Hemorrhagic diathesis

  • Severe anemia

  • Renal and post-renal anuria.

20-25% Albumin (Human) is relatively low in electrolytes compared to the 4-5% Albumin (Human) solutions. When albumin is given, monitor the electrolyte status of the patient and take appropriate steps to restore or maintain the electrolyte balance.



Coagulation Abnormalities


If comparatively large volumes are to be replaced, monitoring of coagulation and hematocrit is necessary. Ensure adequate substitution of other blood constituents (coagulation factors, electrolytes, platelets and erythrocytes).



Laboratory Monitoring


If Albumin (Human) 20% is to be administered, monitor hemodynamic performance regularly; this may include:


  • Arterial blood pressure and pulse rate

  • Central venous pressure

  • Pulmonary artery occlusion pressure

  • Urine output

  • Electrolytes

  • Hematocrit/hemoglobin.

Albumin (Human) 20% must not be diluted with sterile water for injection as this may cause hemolysis in recipients.



Infection Risk from Human Plasma


This product is a derivative of human plasma. Based on effective donor screening and product manufacturing processes it carries an extremely remote risk for transmission of viral diseases. A theoretical risk for transmission of Creutzfeldt-Jakob Disease (CJD) also is considered extremely remote. No cases of transmission of viral diseases or CJD have been identified for Albumin (Human) 20%.



Adverse Reactions



General


The most serious events are anaphylactic shock, circulatory failure, cardiac failure, and pulmonary edema.


The most common adverse events are anaphylactoid type of reactions.


Adverse reactions for Albumin (Human) 20% normally resolve when the infusion rate is slowed down or the infusion is stopped. In case of severe reactions, the infusion should be stopped and appropriate treatment should be initiated.



Clinical Studies Experience


No clinical studies were done using Albumin (Human) 20%



Postmarketing Experience


The following adverse reactions have been identified during post-approval use of Albumin (Human) (any strength). Because these reactions are reported voluntarily from a population of unknown size, it is not always possible to reliably estimate their frequency.


Table 1 Adverse reactions observed for ALBUMIN HUMAN (any strength) during post-marketing phase (in decreasing order of severity)



























Observed Adverse Reactions

anaphylactic shock



cardiac failure



loss of consciousness



circulatory failure



hypersensitivity



congestive heart failure



pulmonary edema



dyspnea



hypotension



hypertension



tachycardia



bradycardia



vomiting



urticaria



angioneurotic edema



rash erythematous



confusional state



headache



chills



pyrexia



flushing



nausea



pruritus



hyperhidrosis


No drug interaction studies have been conducted.



Drug Interactions


No drug interaction studies have been conducted.



USE IN SPECIFIC POPULATIONS



Pregnancy


Pregnancy Category C. Animal reproduction studies have not been performed with Albumin (Human) 20%. It is also not known whether Albumin (Human) 20% can cause fetal harm when administered to a pregnant woman or can affect reproductive capacity. Albumin (Human) 20% should be given to a pregnant woman only if necessary.



Labor and Delivery


It is also not known whether Albumin (Human) 20% can cause fetal harm when administered to a woman during labor or delivery of if it will affect reproductive capacity. Albumin (Human) 20% should be given during labor or delivery only if necessary.



Nursing Mothers


It is not known whether this drug is excreted in human milk. Albumin (Human) 20% should be given to nursing mothers only if necessary. Because many drugs are excreted in human milk, caution should be exercised when Albumin (Human) 20% is administered to a lactating woman.



Pediatric Use


Data on the use of Albumin (Human) 20% in children including premature babies are very limited. The product should be administered to pediatric patients only if needed.



Geriatric Use


Clinical studies did not include a sufficient number of subjects aged 65 and older to determine whether they respond differently from younger subjects.



Albumin (Human) Description


Albumin (Human) 20% is a sterile, liquid preparation of albumin derived from large pools of human plasma. All units of human plasma used in the manufacture of Albumin (Human) 20% are provided by FDA approved blood establishments only.


The product is manufactured by cold ethanol fractionation followed by ultra- and diafiltration. The manufacturing process includes final container pasteurization and additional bulk pasteurization at 60 +/- 0.5°C for 10 – 11 hours. The Albumin (Human) 20% manufacturing process provides a significant viral reduction in in vitro studies (table 2). These reductions are achieved through a combination of process steps including Cohn fractionation and final container pasteurization.


No procedure, however, has been shown to be completely effective in removing viral infectivity from derivatives of human plasma.[see Warnings and Precautions, Infection Risk from Human Plasma (5.7)]


Table 2 In vitro reduction factor during Albumin (Human) 20% manufacturing



PRV:Pseudorabies Virus


SBV: Sindbis Virus


HIV-1:Human Immunodeficiency Virus - 1


Reo 3:Reovirus Type 3


PPV:Porcine Parvovirus


HAV:Hepatitis A Virus


Albumin (Human) 20% is a clear, slightly viscous liquid; it is almost colorless or slightly yellow or green.


The composition of Albumin (Human) 20% is as follows:


























ComponentQuantity/1000 ml

Protein, of which greater than or equal to



96% is human albumin



200 g



Sodium



130 – 160 mmol



Potassium



less than or equal to 2 mmol



N-acetyl-DL-tryptophan



0.064 - 0.096 mmol/g protein



Caprylic acid



0.064 - 0.096 mmol/g protein



Water for Injection



ad. 1000 ml


Albumin (Human) 20% contains no preservatives and components used in its packaging are latex-free.



Albumin (Human) - Clinical Pharmacology


No pharmacokinetic or pharmacodynamic studies with Albumin (Human) 20% have been conducted.



Mechanism of Action


Albumin is responsible for 75-80% of the colloid osmotic pressure of normal plasma. Albumin stabilizes circulating blood volume and is a carrier of hormones, enzymes, medicinal products and toxins. [3 ]


Albumin is a protein with a total extravascular mass of approximately 160 g and an intravascular mass of about 120 g. [3 ]



Pharmacodynamics


The colloid osmotic effect of Albumin (Human) 20% and 25% is approximately 5 times the volume administered. When injected intravenously, it will increase circulating plasma volume by approximately 3.5 times the volume infused within 15 minutes if the patient is adequately hydrated. This extra fluid reduces hemoconcentration and blood viscosity. The degree and duration of volume expansion depends upon the initial blood volume. When treating patients with diminished blood volume, the effect of infused albumin may persist for many hours. The hemodilution lasts for a shorter time when albumin is administered to individuals with normal blood volume. [4 ]



NON-CLINICAL TOXICOLOGY


No non-clinical toxicology studies with Albumin (Human) 20% have been conducted. Human Albumin is a normal constituent of human plasma and acts like physiological albumin.



Clinical Studies


No clinical studies with Albumin (Human) 20% have been conducted.



REFERENCES


  1. Tullis JL: Albumin 2.Guidelines for Clinical Use. JAMA 1977; 237:460-463

  2. Vermeulen LC et al.: A Paradigm for Consensus. Arch. Intern. Med. 1995; 155:373-379

  3. Mendez CM, McClain CJ, Marsano LS: Albumin Therapy in Clinical Practice. Nutrition in Clinical Practice 2005; 20: 314-320

  4. Janeway, C. A. "Human Serum Albumin: Historical Review" in: Proceedings of the Workshop on Albumin. DHEW Publication No. (NIH) 76-925. Sgouris, J. T. and René A. (eds.), Washington, D.C., U.S. Government Printing Office. 1976, pp 3-21.

  5. Martin GS et al.: A randomized, controlled trail of furosemide with or without albumin in hypoproteinemic patients with acute lung injury. Crit. Care Med. 2005; 33: 1681-1687

  6. Tsao YC, Yu VY: Albumin in management of neonatal hyperbilirubinaemia. Arch Dis.Child 1972;47:250-256.

  7. Practice Committee of the American Society for Reproductive Medicine. Ovarian hyperstimulation syndrome. Fertil.Steril. 2006;86:S178-S183.

  8. Aboulghar M, Evers JH, Al Inany H: Intravenous albumin for preventing severe ovarian hyperstimulation syndrome: a Cochrane review. Hum.Reprod. 2002;17:3027-3032.


How Supplied/Storage and Handling


Albumin (Human) 20% is supplied in 10 g in 50 mL or 20 g in 100 mL single use bottles.


















NDC NumberNDC NumberSizeGrams protein

Octapharma Pharmazeutika Produktionsges.m.b.H



Octapharma AB



67467-633-01



68209-633-01



50 ml



10



67467-633-02



68209-633-02



100 ml



20


Albumin (Human) 20% may be stored for 36 months at +2°C to + 25°C (36°F to 77°F) from the date of manufacture.


Store protected from light.


Do not freeze.


Do not use after expiration date.


Do not use if turbid.



Patient Counseling Information



Information for Patients


This product is usually given in a hospital setting.


Inform patients being treated with Albumin (Human) 20% about the potential risks and benefits with its use [see Adverse Reactions (6)].


Discontinue immediately if allergic symptoms occur (e.g. skin rashes, hives, itching, breathing difficulties, coughing, nausea, vomiting, fall in blood pressure, increased heart rate).


Inform patients that Albumin (Human) 20% is a derivative of human plasma and may contain infectious agents that cause disease (e.g., viruses, and theoretically, CJD agent). Inform patients that the risk that Albumin (Human) 20% may transmit an infections agent has been reduced by screening plasma donors for prior exposure for certain viruses, by testing the donated plasma for certain virus infections and by inactivating and/or removing certain viruses during manufacturing [see Warnings and Precautions (5.7)].


Manufactured by:


Octapharma Pharmazeutika Produktionsges.m.b.H.


Oberlaaer Strasse 235


A-1100 Vienna, Austria


Octapharma AB


Elersvägen 40


SE- 112 75, Sweden


U.S. License No. 1646


Distributed by:


Octapharma USA Inc.


121 River Street, 12 th floor









Albumin (Human) 20% 
albumin human  solution










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)67467-633
Route of AdministrationIntravenousDEA Schedule    








Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Albumin (Human) (Albumin (Human))Albumin (Human)200 g  in 1000 mL





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains      














Packaging
#NDCPackage DescriptionMultilevel Packaging
167467-633-0150 mL In 1 BOTTLE, GLASSNone
267467-633-02100 mL In 1 BOTTLE, GLASSNone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA12515410/17/2006


Labeler - Octapharma Pharmazeutika Produktionsgesellschaft m.b.H. (301119178)
Revised: 12/2009Octapharma Pharmazeutika Produktionsgesellschaft m.b.H.

More Albumin (Human) resources


  • Albumin (Human) Use in Pregnancy & Breastfeeding
  • Albumin (Human) Support Group
  • 0 Reviews for Albumin (Human) - Add your own review/rating


Compare Albumin (Human) with other medications


  • Burns, External
  • Hypoproteinemia
  • Pancreatitis
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Tuesday, 10 July 2012

AK-Neo-Dex


Generic Name: neomycin and dexamethasone ophthalmic (nee oh MYE sin DEX a METH a sone off THAL mik)

Brand Names:


What is AK-Neo-Dex (neomycin and dexamethasone ophthalmic)?

Neomycin is an antibiotic. It is used to treat bacterial infections.


Dexamethasone is a steroid. It is used to treat the inflammation associated with bacterial infections of the eye.


Neomycin and dexamethasone ophthalmic is used to treat bacterial infections of the eyes.

Neomycin and dexamethasone ophthalmic may also be used for purposes other than those listed in this medication guide.


What is the most important information I should know about AK-Neo-Dex (neomycin and dexamethasone ophthalmic)?


Contact your doctor if your symptoms begin to get worse or if you do not see any improvement in your condition after a few days.


Do not touch the dropper or tube opening to any surface, including your eyes or hands. The dropper or tube opening is sterile. If it becomes contaminated, it could cause an infection in your eye.

Apply light pressure to the inside corner of your eye (near your nose) after each drop to prevent the fluid from draining down your tear duct.


Who should not use AK-Neo-Dex (neomycin and dexamethasone ophthalmic)?


Do not use neomycin and dexamethasone ophthalmic if you have a viral or fungal infection in your eye. It is used to treat infections caused by bacteria only. Neomycin and dexamethasone ophthalmic is in the FDA pregnancy category C. This means that it is not known whether it will harm an unborn baby. Do not use this medication without first talking to your doctor if you are pregnant. It is also not known whether neomycin and dexamethasone ophthalmic passes into breast milk. Do not use this medication without first talking to your doctor if you are breast-feeding a baby.

How should I use AK-Neo-Dex (neomycin and dexamethasone ophthalmic)?


Use neomycin and dexamethasone ophthalmic eyedrops or ointment exactly as directed by your doctor. If you do not understand these directions, ask your pharmacist, nurse, or doctor to explain them to you.


Wash your hands before and after using your eyedrops or ointment.

To apply the eyedrops:



  • Tilt your head back slightly and pull down on your lower eyelid. Position the dropper above your eye. Look up and away from the dropper. Squeeze out a drop and close your eye. Apply gentle pressure to the inside corner of your eye (near your nose) for about 1 minute to prevent the liquid from draining down your tear duct. Repeat the process in the other eye if your doctor has prescribed drops in both eyes. If you are using more than one drop in the same eye, repeat the process with about 5 minutes between drops.



To apply the ointment:



  • Hold the tube in your hand for a few minutes to warm it up so that the ointment comes out easily. Tilt your head back slightly and pull down gently on your lower eyelid. Apply a thin film of the ointment into your lower eyelid. Close your eye and roll your eyeball around in all directions for 1 to 2 minutes. Repeat the process in the other eye if your doctor has prescribed ointment in both eyes.



If you are applying another eye medication, allow at least 10 minutes before your next application.


Do not touch the dropper or tube opening to any surface, including your eyes or hands. The dropper or tube opening is sterile. If it becomes contaminated, it could cause an infection in your eye. Do not use any eyedrop that is discolored or has particles in it. Store neomycin and dexamethasone ophthalmic at room temperature away from moisture and heat. Keep the bottle or tube properly capped.

What happens if I miss a dose?


Apply the missed dose as soon as you remember. However, if it is almost time for your next regularly scheduled dose, skip the missed dose and apply the next one as directed. Do not use a double dose of this medication.


What happens if I overdose?


An overdose of this medication is unlikely to occur. If you do suspect an overdose, wash the eye with water and call an emergency room or poison control center near you. If the drops or ointment have been ingested, drink plenty of fluid and call an emergency center for advice.


What should I avoid while using AK-Neo-Dex (neomycin and dexamethasone ophthalmic)?


Do not touch the dropper or tube opening to any surface, including your eyes or hands. The dropper or tube opening is sterile. If it becomes contaminated, it could cause an infection in your eye. Use caution when driving, operating machinery, or performing other hazardous activities. Neomycin and dexamethasone ophthalmic may cause blurred vision. If you experience blurred vision, avoid these activities.

Use caution with contact lenses. Wear them only if your doctor approves. After applying this medication, wait at least 15 minutes before inserting contact lenses.


Avoid other eye medications unless your doctor approves.


AK-Neo-Dex (neomycin and dexamethasone ophthalmic) side effects


Serious side effects are not expected with this medication.


Some burning, stinging, irritation, itching, redness, blurred vision, eyelid itching, eyelid swelling, or sensitivity to light may occur.


This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.


What other drugs will affect AK-Neo-Dex (neomycin and dexamethasone ophthalmic)?


Avoid other eye medications unless they are approved by your doctor.


Before using this medication, tell your doctor if you are taking an oral steroid medication such as prednisone (Deltasone, Orasone, others).


Drugs other than those listed here may also interact with neomycin and dexamethasone ophthalmic. Talk to your doctor and pharmacist before taking any prescription or over-the-counter medicines.



More AK-Neo-Dex resources


  • AK-Neo-Dex Side Effects (in more detail)
  • AK-Neo-Dex Use in Pregnancy & Breastfeeding
  • AK-Neo-Dex Drug Interactions
  • AK-Neo-Dex Support Group
  • 0 Reviews for AK-Neo-Dex - Add your own review/rating


Compare AK-Neo-Dex with other medications


  • Blepharitis
  • Conjunctivitis, Bacterial
  • Keratitis
  • Keratoconjunctivitis
  • Uveitis


Where can I get more information?


  • Your pharmacist has additional information about neomycin and dexamethasone ophthalmic written for health professionals that you may read.

See also: AK-Neo-Dex side effects (in more detail)


Monday, 9 July 2012

Alimta


Generic Name: pemetrexed (Intravenous route)

pem-e-TREX-ed

Commonly used brand name(s)

In the U.S.


  • Alimta

Available Dosage Forms:


  • Powder for Solution

Therapeutic Class: Antineoplastic Agent


Uses For Alimta


Pemetrexed injection treats lung cancer and belongs to the group of medicines called antineoplastics. It is used together with cisplatin (a cancer medicine) to treat a type of cancer called malignant pleural mesothelioma (MPM). This cancer affects the inside lining of the chest cavity. Pemetrexed injection may also be used alone or together with cisplatin to treat a type of lung cancer called nonsquamous non-small cell lung cancer.


To lower your chances of side effects with pemetrexed, you must also take folic acid and vitamin B12 prior to and during your treatment. Your doctor will prescribe a medicine called a corticosteroid (cortisone medicine) to take for 3 days during your treatment. Corticosteroid medicines lower your chances of getting skin reactions with pemetrexed.


This medicine is available only with your doctor's prescription.


Before Using Alimta


In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.


Pediatric


Appropriate studies have been performed on the relationship of age to the effects of pemetrexed injection in the pediatric population. However, efficacy has not been established.


Geriatric


Appropriate studies performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of pemetrexed injection in the elderly. However, elderly patients are more likely to have age-related kidney problems, which may require an adjustment in the dose for patients receiving pemetrexed injection.


Pregnancy








Pregnancy CategoryExplanation
All TrimestersDStudies in pregnant women have demonstrated a risk to the fetus. However, the benefits of therapy in a life threatening situation or a serious disease, may outweigh the potential risk.

Breast Feeding


There are no adequate studies in women for determining infant risk when using this medication during breastfeeding. Weigh the potential benefits against the potential risks before taking this medication while breastfeeding.


Interactions with Medicines


Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. When you are receiving this medicine, it is especially important that your healthcare professional know if you are taking any of the medicines listed below. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.


Using this medicine with any of the following medicines is usually not recommended, but may be required in some cases. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.


  • Aceclofenac

  • Acemetacin

  • Alclofenac

  • Apazone

  • Benoxaprofen

  • Bromfenac

  • Bufexamac

  • Carprofen

  • Celecoxib

  • Clometacin

  • Clonixin

  • Dexketoprofen

  • Diclofenac

  • Diflunisal

  • Dipyrone

  • Droxicam

  • Etodolac

  • Etofenamate

  • Felbinac

  • Fenbufen

  • Fenoprofen

  • Fentiazac

  • Floctafenine

  • Flufenamic Acid

  • Flurbiprofen

  • Ibuprofen

  • Indomethacin

  • Indoprofen

  • Isoxicam

  • Ketoprofen

  • Ketorolac

  • Lornoxicam

  • Meclofenamate

  • Mefenamic Acid

  • Meloxicam

  • Nabumetone

  • Naproxen

  • Niflumic Acid

  • Nimesulide

  • Oxaprozin

  • Oxyphenbutazone

  • Phenylbutazone

  • Pirazolac

  • Piroxicam

  • Pirprofen

  • Propyphenazone

  • Proquazone

  • Rofecoxib

  • Sulindac

  • Suprofen

  • Tenidap

  • Tenoxicam

  • Tiaprofenic Acid

  • Ticrynafen

  • Tolmetin

  • Zomepirac

Interactions with Food/Tobacco/Alcohol


Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. Discuss with your healthcare professional the use of your medicine with food, alcohol, or tobacco.


Other Medical Problems


The presence of other medical problems may affect the use of this medicine. Make sure you tell your doctor if you have any other medical problems, especially:


  • Ascites (extra fluid in your stomach area) or

  • Bone marrow problems (e.g., anemia, neutropenia, thrombocytopenia)—Use with caution. May make these conditions worse.

  • Kidney disease or

  • Liver disease—Use with caution. The effects may be increased because of slower removal of pemetrexed from the body.

  • Kidney disease, severe—Should not be given in patients with this condition.

Proper Use of Alimta


It is very important to take folic acid and vitamin B12 during your treatment with pemetrexed to lower your chances of harmful side effects. You must start taking 350-1000 micrograms of folic acid every day for at least 5 days out of the 7 days before your first dose of pemetrexed. You must keep taking folic acid every day during the time you are getting treatment with pemetrexed, and for 21 days after your last treatment. You can get folic acid vitamins over-the-counter. Folic acid is also found in many multivitamin pills. Ask your doctor or pharmacist for help if you are not sure how to choose a folic acid product. Your doctor will give you vitamin B12 injections while you are getting treatment with pemetrexed. You will get your first vitamin B12 injection during the week before your first dose of pemetrexed, and then about every 9 weeks during treatment.


You will receive this medicine while you are in a hospital or cancer treatment center. A nurse or other trained health professional will give you this medicine. This medicine is given through a needle placed in one of your veins.


Pemetrexed is given together with certain other medicines. If you are using a combination of medicines, it is important that you receive each one at the proper time. If you are taking some of these medicines by mouth, ask your doctor to help you create a plan to take them at the right times.


Your doctor will prescribe a medicine called a corticosteroid (cortisone medicine) to take for 3 days during your treatment with pemetrexed. Corticosteroid medicines lower your chances for getting skin reactions with pemetrexed.


This medicine comes with a patient information insert. It is very important that you read and understand this information. Be sure to ask your doctor about anything you do not understand.


Precautions While Using Alimta


It is very important that your doctor check your progress at regular visits to make sure this medicine is working properly. Blood tests may be needed to check for unwanted effects.


Make sure your doctor knows if you are pregnant before you receive this medicine. Using this medicine while you are pregnant can harm your unborn baby. If you are a woman of childbearing potential, you should use two forms of birth control together to avoid getting pregnant while you are receiving this medicine. If you have become pregnant during your treatment, tell your doctor right away.


It is important that you check with your doctor right away if you have fever or chills, diarrhea, or mouth sores. These may be signs that you have an infection.


You may feel tired or weak for a few days after your pemetrexed treatment. If you have severe weakness or tiredness, call your doctor.


You may get redness or sores in your mouth, throat, or lips. These symptoms may happen a few days after pemetrexed treatment.


You may get a rash or itching during treatment. These usually appear between treatments with pemetrexed and usually go away before the next treatment. Call your doctor if you get a severe rash or itching.


Pemetrexed and cisplatin (a cancer medicine) can sometimes cause nausea and vomiting. However, it is very important that you continue to receive the medicine, even if you begin to feel ill. You can get medicines to help control the nausea and vomiting. Talk with your doctor if you get any of these symptoms.


You may lose your appetite and some weight during your treatment. Talk to your doctor if this is a problem for you.


While you are being treated with pemetrexed, and after you stop treatment with it, do not have any immunizations (vaccinations) without your doctor's approval. Pemetrexed may lower your body's resistance and there is a chance you might get the infection the immunization is meant to prevent. In addition, other persons living in your household should not take oral polio vaccine since there is a chance they could pass the polio virus on to you. Also, avoid other persons who have taken oral polio vaccine within the last several months. Do not get close to them, and do not stay in the same room with them for very long. If you cannot take these precautions, you should consider wearing a protective face mask that covers the nose and mouth.


Pemetrexed can temporarily affect your blood counts and your doctor will do blood tests to check your blood counts before and during treatment with pemetrexed. Low red blood cells may make you feel tired, get tired easily, appear pale, and become short of breath. Low white blood cells may give you a greater chance for infection. If you have a fever (temperature above 100.4 degrees F) or other signs of infection, call your doctor right away. Low platelets give you a greater chance for bleeding. If this occurs, there are certain precautions you can take, especially when your blood count is low, to reduce the risk of infection or bleeding:


  • If you can, avoid people with infections. Check with your doctor immediately if you think you are getting an infection or if you get a fever or chills, cough or hoarseness, diarrhea, lower back or side pain, mouth sores, or painful or difficult urination.

  • Check with your doctor immediately if you notice any unusual bleeding or bruising; black, tarry stools; blood in the urine or stools; or pinpoint red spots on your skin.

  • Be careful when using a regular toothbrush, dental floss, or toothpick. Your medical doctor, dentist, or nurse may recommend other ways to clean your teeth and gums. Check with your medical doctor before having any dental work done.

  • Do not touch your eyes or the inside of your nose unless you have just washed your hands and have not touched anything else in the meantime.

  • Be careful not to cut yourself when you are using sharp objects such as a safety razor or fingernail or toenail cutters.

  • Avoid contact sports or other situations where bruising or injury could occur.

Make sure your doctor knows if you are also using a pain or arthritis medicine (e.g., ibuprofen, Motrin®) while you are receiving this medicine. These medicines should be used with caution in patients with kidney problems.


Do not take other medicines unless they have been discussed with your doctor. This includes prescription or nonprescription (over-the-counter [OTC]) medicines and herbal or vitamin supplements.


Alimta Side Effects


Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.


Check with your doctor or nurse immediately if any of the following side effects occur:


More common
  • Black, tarry stools

  • bleeding gums

  • chest pain

  • chills

  • cough

  • fever

  • loss of coordination

  • lower back or side pain

  • painful or difficult urination

  • pains in the chest, groin, or legs, especially calves of the legs

  • pale skin

  • pinpoint red spots on the skin

  • severe headaches of sudden onset

  • shortness of breath

  • sore throat

  • sudden onset of slurred speech

  • sudden vision changes

  • swollen glands

  • troubled breathing

  • ulcers, sores, or white spots in the mouth

  • unusual bleeding or bruising

  • unusual tiredness or weakness

Less common
  • Bloody urine or bloody stools

  • decreased frequency or amount of urine

  • fainting or loss of consciousness

  • fast or irregular breathing

  • increased blood pressure

  • increased thirst

  • itching

  • loss of appetite

  • nausea

  • skin rash

  • swelling of the eyes or eyelids

  • swelling of the face, fingers, or lower legs

  • tightness in the chest or wheezing

  • vomiting

  • weight gain

Incidence not known
  • Blistering, peeling, or loosening of the skin

  • joint or muscle pain

  • pain and redness of the skin in the area of earlier radiation treatment

  • red skin lesions, often with a purple center

  • red, irritated eyes

  • stomach cramps, tenderness, or pain

  • watery diarrhea

Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:


More common
  • Burning, tingling, numbness, or pain in the hands, arms, feet, or legs

  • confusion

  • cough or hoarseness

  • decreased urination

  • diarrhea (without colostomy)

  • difficulty having a bowel movement (stool)

  • difficulty with moving

  • difficulty with swallowing

  • discouragement

  • dizziness

  • dry mouth

  • feeling sad or empty

  • hair loss

  • headache

  • heartburn

  • increase in heart rate

  • irritability

  • lightheadedness

  • loss of interest or pleasure

  • mood changes

  • muscle aches or cramping

  • muscle stiffness

  • pain or burning in the throat

  • pain produced by swallowing

  • rapid breathing

  • sensation of pins and needles

  • stabbing pain

  • stuffy or runny nose

  • sunken eyes

  • swelling

  • swelling or inflammation of the mouth

  • swollen joints

  • thinning of the hair

  • thirst

  • tiredness

  • trouble concentrating

  • trouble sleeping

  • weight loss

  • wheezing

  • wrinkled skin

Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.


Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.

See also: Alimta side effects (in more detail)



The information contained in the Thomson Reuters Micromedex products as delivered by Drugs.com is intended as an educational aid only. It is not intended as medical advice for individual conditions or treatment. It is not a substitute for a medical exam, nor does it replace the need for services provided by medical professionals. Talk to your doctor, nurse or pharmacist before taking any prescription or over the counter drugs (including any herbal medicines or supplements) or following any treatment or regimen. Only your doctor, nurse, or pharmacist can provide you with advice on what is safe and effective for you.


The use of the Thomson Reuters Healthcare products is at your sole risk. These products are provided "AS IS" and "as available" for use, without warranties of any kind, either express or implied. Thomson Reuters Healthcare and Drugs.com make no representation or warranty as to the accuracy, reliability, timeliness, usefulness or completeness of any of the information contained in the products. Additionally, THOMSON REUTERS HEALTHCARE MAKES NO REPRESENTATION OR WARRANTIES AS TO THE OPINIONS OR OTHER SERVICE OR DATA YOU MAY ACCESS, DOWNLOAD OR USE AS A RESULT OF USE OF THE THOMSON REUTERS HEALTHCARE PRODUCTS. ALL IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE OR USE ARE HEREBY EXCLUDED. Thomson Reuters Healthcare does not assume any responsibility or risk for your use of the Thomson Reuters Healthcare products.


More Alimta resources


  • Alimta Side Effects (in more detail)
  • Alimta Use in Pregnancy & Breastfeeding
  • Alimta Drug Interactions
  • Alimta Support Group
  • 0 Reviews for Alimta - Add your own review/rating


  • Alimta Prescribing Information (FDA)

  • Alimta Consumer Overview

  • Alimta Monograph (AHFS DI)

  • Alimta MedFacts Consumer Leaflet (Wolters Kluwer)

  • Pemetrexed Professional Patient Advice (Wolters Kluwer)



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Saturday, 7 July 2012

Proventil HFA



albuterol sulfate

Dosage Form: inhalation aerosol
PROVENTIL® HFA

(albuterol sulfate)

Inhalation Aerosol

FOR ORAL INHALATION ONLY


Prescribing Information



DESCRIPTION


The active component of PROVENTIL® HFA (albuterol sulfate) Inhalation Aerosol is albuterol sulfate, USP racemic α1 [(tert-Butylamino)methyl]-4-hydroxy-m-xylene-α,α'-diol sulfate (2:1)(salt), a relatively selective beta2-adrenergic bronchodilator having the following chemical structure:



Albuterol sulfate is the official generic name in the United States. The World Health Organization recommended name for the drug is salbutamol sulfate. The molecular weight of albuterol sulfate is 576.7, and the empirical formula is (C13H21 NO3)2•H2SO4. Albuterol sulfate is a white to off-white crystalline solid. It is soluble in water and slightly soluble in ethanol. Proventil HFA Inhalation Aerosol is a pressurized metered-dose aerosol unit for oral inhalation. It contains a microcrystalline suspension of albuterol sulfate in propellant HFA-134a (1,1,1,2-tetrafluoroethane), ethanol, and oleic acid.


Each actuation delivers 120 mcg albuterol sulfate, USP from the valve and 108 mcg albuterol sulfate, USP from the mouthpiece (equivalent to 90 mcg of albuterol base from the mouthpiece). Each canister provides 200 inhalations. It is recommended to prime the inhaler before using for the first time and in cases where the inhaler has not been used for more than 2 weeks by releasing four “test sprays” into the air, away from the face.


This product does not contain chlorofluorocarbons (CFCs) as the propellant.



CLINICAL PHARMACOLOGY



Mechanism of Action  In vitro studies and in vivo pharmacologic studies have demonstrated that albuterol has a preferential effect on beta2-adrenergic receptors compared with isoproterenol. While it is recognized that beta2-adrenergic receptors are the predominant receptors on bronchial smooth muscle, data indicate that there is a population of beta2-receptors in the human heart existing in a concentration between 10% and 50% of cardiac beta-adrenergic receptors. The precise function of these receptors has not been established. (See WARNINGS, Cardiovascular Effects section.)


Activation of beta2-adrenergic receptors on airway smooth muscle leads to the activation of adenylcyclase and to an increase in the intra-cellular concentration of cyclic-3',5'-adenosine monophosphate (cyclic AMP). This increase of cyclic AMP leads to the activation of protein kinase A, which inhabits the phosphorylation of myosin and lowers intracellular ionic calcium concentrations, resulting in relaxation. Albuterol relaxes the smooth muscles of all airways, from the trachea to the terminal bronchioles. Albuterol acts as a functional antagonist to relax the airway irrespective of the spasmogen involved, thus protecting against all bronchoconstricor challenges. Increased cyclic AMP concentrations are also associated with the inhibition of release of mediators from mast cells in the airway.


Albuterol has been shown in most clinical trials to have more effect on the respiratory tract, in the form of bronchial smooth muscle relaxation, than isoproterenol at comparable doses while producing fewer cardiovascular effects. Controlled clinical studies and other clinical experience have shown that inhaled albuterol, like other beta-adrenergic agonist drugs, can produce a significant cardiovascular effect in some patients, as measured by pulse rate, blood pressure, symptoms, and/or electrocardiographic changes.



Preclinical  Intravenous studies in rats with albuterol sulfate have demonstrated that albuterol crosses the blood-brain barrier and reaches brain concentrations amounting to approximately 5% of the plasma concentrations. In structures outside the blood-brain barrier (pineal and pituitary glands), albuterol concentrations were found to be 100 times those in the whole brain.


Studies in laboratory animals (minipigs, rodents, and dogs) have demonstrated the occurrence of cardiac arrhythmias and sudden death (with histologic evidence of myocardial necrosis) when beta2-agonist and methylxanthines were administered concurrently. The clinical significance of these findings is unknown.


Propellant HFA-134a is devoid of pharmacological activity except at very high doses in animals (380-1300 times the maximum human exposure based on comparisons of AUC values), primarily producing ataxia, tremors, dyspnea, or salivation. These are similar to effects produced by the structurally related chlorofluorocarbons (CFCs), which have been used extensively in metered dose inhalers.


In animals and humans, propellant HFA-134a was found to be rapidly absorbed and rapidly eliminated, with an elimination half-life of 3 to 27 minutes in animals and 5 to 7 minutes in humans. Time to maximum plasma concentration (Tmax) and mean residence time are both extremely short, leading to a transient appearance of HFA-134a in the blood with no evidence of accumulation.



Pharmacokinetics  In a single-dose bioavailability study which enrolled six healthy, male volunteers, transient low albuterol levels (close to the lower limit of quantitation) were observed after administration of two puffs from both PROVENTIL® HFA Inhalation Aerosol and a CFC 11/12 propelled albuterol inhaler. No formal pharmacokinetic analyses were possible for either treatment, but systemic albuterol levels appeared similar.



Clinical Trials  In a 12-week, randomized, double-blind, double-dummy, active- and placebo-controlled trial, 565 patients with asthma were evaluated for the bronchodilator efficacy of Proventil HFA Inhalation Aerosol (193 patients) in comparison to a CFC 11/12 propelled albuterol inhaler (186 patients) and an HFA-134a placebo inhaler (186 patients).


Serial FEV1 measurements (shown below as percent change from test-day baseline) demonstrated that two inhalations of Proventil HFA Inhalation Aerosol produced significantly greater improvement in pulmonary function than placebo and produced outcomes which were clinically comparable to a CFC 11/12 propelled albuterol inhaler.


The mean time to onset of a 15% increase in FEV1 was 6 minutes and the mean time to peak effect was 50 to 55 minutes. The mean duration of effect as measured by a 15% increase in FEV1 was 3 hours. In some patients, duration of effect was as long as 6 hours.


In another clinical study in adults, two inhalations of Proventil HFA Inhalation Aerosol taken 30 minutes before exercise prevented exercise-induced bronchospasm as demonstrated by the maintenance of FEV1 within 80% of baseline values in the majority of patients.


In a 4-week, randomized, open-label trial, 63 children, 4 to 11 years of age, with asthma were evaluated for the bronchodilator efficacy of Proventil HFA Inhalation Aerosol (33 pediatric patients) in comparison to a CFC 11/12 propelled albuterol inhaler (30 pediatric patients).



Serial FEV1 measurements as percent change from test-day baseline demonstrated that two inhalations of Proventil HFA Inhalation Aerosol produced outcomes which were clinically comparable to a CFC 11/12 propelled albuterol inhaler.


The mean time to onset of a 12% increase in FEV1 for Proventil HFA Inhalation Aerosol was 7 minutes and the mean time to peak effect was approximately 50 minutes. The mean duration of effect as measured by a 12% increase in FEV1 was 2.3 hours. In some pediatric patients, duration of effect was as long as 6 hours.


In another clinical study in pediatric patients, two inhalations of Proventil HFA Inhalation Aerosol taken 30 minutes before exercise provided comparable protection against exercise-induced bronchospasm as a CFC 11/12 propelled albuterol inhaler.



INDICATIONS AND USAGE


PROVENTIL® HFA Inhalation Aerosol is indicated in adults and children 4 years of age and older for the treatment or prevention of bronchospasm with reversible obstructive airway disease and for the prevention of exercise-induced bronchospasm.



CONTRAINDICTIONS


PROVENTIL® HFA Inhalation Aerosol is contraindicated in patients with a history of hypersensitivity to albuterol or any other Proventil HFA components.



WARNINGS


  1. Paradoxical Bronchospasm: Inhaled albuterol sulfate can produce paradoxical bronchospasm that may be life threatening. If paradoxical bronchospasm occur, PROVENTIL® HFA Inhalation Aerosol should be discontinued immediately and alternative therapy instituted. It should be recognized that paradoxical bronchospasm, when associated with inhaled formulations, frequently occurs with the first use of a new canister.

  2. Deterioration of Asthma: Asthma may deteriorate acutely over a period of hours or chronically over several days or longer. If the patient needs more doses of Proventil HFA Inhalation Aerosol than usual, this may be a marker of destabilization of asthma and requires re-evaluation of the patient and treatment regimen, giving special consideration to the possible need for anti-inflammatory treatment, eg, corticosteroids.

  3. Use of Anti-inflammatory Agents: The use of beta-adrenergic-agonist bronchodilators alone may not be adequate to control asthma in many patients. Early consideration should be given to adding anti-inflammatory agents, eg, corticosteroids, to the therapeutic regimen.

  4. Cardiovascular Effects: Proventil HFA Inhalation Aerosol, like other beta-adrenergic agonist, can produce clinically significant cardiovascular effects in some patients as measured by pulse rate, blood pressure, and/or symptoms. Although such effects are uncommon after administration of Proventil HFA Inhalation Aerosol at recommended doses, if they occur, the drug may need to be discontinued. In addition, beta-agonists have been reported to produce ECG changes, such as flattening of the T wave, prolongation of the QTc interval, and ST segment depression. The clinical significance of these findings is unknown. Therefore, Proventil HFA Inhalation Aerosol, like all sympathomimetic amines, should be used with caution in patients with cardiovascular disorders, especially coronary insufficiency, cardiac arrhythmias, and hypertension.

  5. Do Not Exceed Recommended Dose: Fatalities have been reported in association with excessive use of inhaled sympathomimetic drugs in patients with asthma. The exact cause of death is unknown, but cardiac arrest following an unexpected development of a severe acute asthmatic crisis and subsequent hypoxia is suspected.

  6. Immediate Hypersensitivity Reactions: Immediate hypersensitivity reactions may occur after administration of albuterol sulfate, as demonstrated by rare cases of urticaria, angioedema, rash, bronchospasm, anaphylaxis, and oropharyngeal edema.


PRECAUTIONS



General Albuterol sulfate, as with all sympathomimetic amines, should be used with caution in patients with cardiovascular disorders, especially coronary insufficiency, cardiac arrhythmias, and hypertension; in patients with convulsive disorders, hyperthyroidism, or diabetes mellitus; and in patients who are unusually responsive to sympathomimetic amines. Clinically significant changes in systolic and diastolic blood pressure have been seen in individual patients and could be expected to occur in some patients after use of any beta-adrenergic bronchodilator.


Large doses of intravenous albuterol have been reported to aggravate preexisting diabetes mellitus and ketoacidosis. As with other beta-agonists, albuterol may produce significant hypokalemia in some patients, possibly through intracellular shunting, which has the potential to produce adverse cardiovascular effects. The decrease is usually transient, not requiring supplementation.



Information for Patients See illustrated Patient's Instructions for Use. SHAKE WELL BEFORE USING. Patients should be given the following information:


It is recommended to prime the inhaler before using for the first time and in cases where the inhaler has not been used for more than 2 weeks by releasing four “test sprays” into the air, away from the face.


KEEPING THE PLASTIC MOUTHPIECE CLEAN IS VERY IMPORTANT TO PREVENT MEDICATION BUILD-UP AND BLOCKAGE. THE MOUTHPIECE SHOULD BE WASHED, SHAKEN TO REMOVE EXCESS WATER, AND AIR DRIED THOROUGHLY AT LEASE ONCE A WEEK. INHALER MAY CEASE TO DELIVER MEDICATION IF NOT PROPERLY CLEANED.


The mouthpiece should be cleaned (with the canister removed) by running warm water through the top and bottom for 30 seconds at least once a week. The mouthpiece must be shaken to remove excess water, then air dried thoroughly (such as overnight). Blockage from medication build-up or improper medication delivery may result from failure to thoroughly air dry the mouthpiece.


If the mouthpiece should become blocked (little or no medication coming out of the mouthpiece), the blockage may be removed by washing as described above.


If it is necessary to use the inhaler before it is completely dry, shake off excess water, replace canister, test spray twice away from face, and take the prescribed dose. After such use, the mouthpiece should be rewashed and allowed to air dry thoroughly.


The action of PROVENTIL® HFA Inhalation Aerosol should last up to 4 to 6 hours. Proventil HFA Inhalation Aerosol should not be used more frequently than recommended. Do not increase the dose or frequency of doses of Proventil HFA Inhalation Aerosol without consulting your physician. If you find that treatment with Proventil HFA Inhalation Aerosol becomes less effective for symptomatic relief, your symptoms become worse, and/or you need to use the product more frequently than usual, medical attention should be sought immediately. While you are taking Proventil HFA Inhalation Aerosol, other inhaled drugs and asthma medications should be taken only as directed by your physician.


Common adverse effects of treatment with inhaled albuterol include palpitations, chest pain, rapid heart rate, tremor, or nervousness. If you are pregnant or nursing, contact your physician about use of Proventil HFA Inhalation Aerosol. Effective and safe use of Proventil HFA Inhalation Aerosol includes an understanding of the way that it should be administered. Use Proventil HFA Inhalation Aerosol only with the actuator supplied with the product. Discard the canister after 200 sprays have been used.


In general, the technique for administering Proventil HFA Inhalation Aerosol to children is similar to that for adults. Children should use Proventil HFA Inhalation Aerosol under adult supervision, as instructed by the patient's physician. (See Patient's Instructions for Use).



Drug Interactions


  1. Beta-Blockers: Beta-adrenergic-receptor blocking agents not only block the pulmonary effect of beta-agonists, such as Proventil HFA Inhalation Aerosol, but may produce severe bronchospasm in asthmatic patients. Therefore, patients with asthma should not normally be treated with beta-blockers. However, under certain circumstances, eg, as prophylaxis after myocardial infarction, there may be no acceptable alternatives to the use of beta-adrenergic blocking agents in patients with asthma. In this setting, cardioselective beta blockers should be considered, although they should be administered with caution.

  2. Diuretics: The ECG changes and/or hypokalemia which may result from the administration of nonpotassium-sparing diuretics (such as loop or thiazide diuretics) can be acutely worsened by beta-agonists, especially when the recommended dose of the beta-agonist is exceeded. Although the clinical significance of these effects is not known, caution is advised in the coadministration of beta agonists with nonpotassium-sparing diuretics.

  3. Albuterol-Digoxin: Mean decreases of 16% and 22% in serum digoxin levels were demonstrated after single-dose intravenous and oral administration of albuterol, respectively, to normal volunteers who had received digoxin for 10 days. The clinical significance of these findings for patients with obstructive airway disease who are receiving albuterol and digoxin on a chronic basis is unclear; nevertheless, it would be prudent to carefully evaluate the serum digoxin levels in patients who are currently receiving digoxin and albuterol.

  4. Monoamine Oxidase Inhibitors or Tricyclic Antidepressants: Proventil HFA Inhalation Aerosol should be administered with extreme caution to patients being treated with monoamine oxidase inhibitors or tricyclic antidepressants, or within 2 weeks of discontinuation of such agents, because the action of albuterol on the cardiovascular system may be potentiated.


Carcinogenesis, Mutagenesis, and Impairment of Fertility


In a 2-year study in SPRAGUE-DAWLEY® rats, albuterol sulfate caused a dose-related increase in the incidence of benign leiomyomas of the mesovarium at the above dietary doses of 2 mg/kg (approximately 15 times the maximum recommended daily inhalation dose for adults on a mg/m2 basis and approximately 6 times the maximum recommended daily inhalation dose for children on a mg/m2 basis). In another study this effect was blocked by the coadministration of propranolol, a nonselective beta-adrenergic antagonist. In an 18-month study in CD-1 mice, albuterol sulfate showed no evidence of tumorigenicity at dietary doses of up to 500 mg/kg (approximately 1700 times the maximum recommended daily inhalation dose for adults on a mg/m2 basis and approximately 800 times the maximum recommended daily inhalation dose for children on a mg/m2 basis). In a 22-month study in Golden Hamsters, albuterol sulfate showed no evidence of tumorigenicity at dietary doses of up to 50 mg/kg (approximately 225 times the maximum recommended daily inhalation dose for adults on a mg/m2 basis and approximately 110 times the maximum recommended daily inhalation dose for children on a mg/m2 basis).


Albuterol sulfate was not mutagenic in the Ames test or a mutation test in yeast. Albuterol sulfate was not clastogenic in a human peripheral lymphocyte assay or in an AH1 strain mouse micronucleus assay.


Reproduction studies in rats demonstrated no evidence of impaired fertility at oral doses up to 50 mg/kg (approximately 340 times the maximum recommended daily inhalation dose for adults on a mg/m2 basis).



Pregnancy: Teratogenic Effects: Pregnancy Category C


Albuterol sulfate has been shown to be teratogenic in mice. A study in CD-1 mice given albuterol sulfate subcutaneously showed cleft palate formation in 5 of 111 (4.5%) fetuses at 0.25 mg/kg (less than the maximum recommended daily inhalation dose for adults on a mg/m2 basis) and in 10 of 108 (9.3%) fetuses at 2.5 mg/kg (approximately 8 times the maximum recommended daily inhalation dose for adults on a mg/m2 basis). The drug did not induce cleft palate formation at a dose of 0.025 mg/kg (less than the maximum recommended daily inhalation dose for adults on a mg/m2 basis). Cleft palate also occurred in 22 of 72 (30.5%) fetuses from females treated subcutaneously with 2.5 mg/kg of isoproterenol (positive control).


A reproduction study in Stride Dutch rabbits revealed cranioschisis in 7 of 19 (37%) fetuses when albuterol sulfate was administered orally at 50 mg/kg dose (approximately 680 times the maximum recommended daily inhalation dose for adults on a mg/m2 basis).


In an inhalation reproduction study in SPRAGUE-DAWLEY rats, the albuterol sulfate/HFA-134a formulation did not exhibit any teratogenic effects at 10.5 mg/kg (approximately 70 times the maximum recommended daily inhalation dose for adults on a mg/m2 basis).


A study in which pregnant rats were dosed with radiolabeled albuterol sulfate demonstrated that drug-related material is transferred from the maternal circulation to the fetus.


There are no adequate and well-controlled studies of Proventil HFA Inhalation Aerosol or albuterol sulfate in pregnant women. Proventil HFA Inhalation Aerosol should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.


During worldwide marketing experience, various congenital anomalies, including cleft palate and limb defects, have been reported in the offspring of patients being treated with albuterol. Some of the mothers were taking multiple medications during their pregnancies. Because no consistent pattern of defects can be discerned, a relationship between albuterol use and congenital anomalies has not been established.



Use in Labor and Delivery


Because of the potential for beta-agonist interference with uterine contractility, use of Proventil HFA Inhalation Aerosol for relief of bronchospesm during labor should be restricted to those patients in whom the benefits clearly outweigh the risk.



Tocolysis: Albuterol has not been approved for the management of preterm labor. The benefit:risk ratio when albuterol is administered for tocolysis has not been established. Serious adverse reactions, including pulmonary edema, have been reported during the following treatment of premature labor with beta2-agonists, including albuterol.



Nursing Mothers


Plasma levels of albuterol sulfate and HFA-134a after inhaled therapeutic doses are very low in humans, but it is not known whether the components of Proventil HFA Inhalation Aerosol are excreated in human milk.


Because of the potential for tumorigenicity shown for albuterol in animal studies and lack of experience with the use of Proventil HFA Inhalation Aerosol by nursing mothers, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother. Caution should be exercised when albuterol sulfate is administered to a nursing woman.



Pediatrics


The safety and effectiveness of Proventil HFA Inhalation Aerosol in pediatric patients below the age of 4 years have not been established.



Geriatrics


Proventil HFA Inhalation Aerosol has not been studied in a geriatric population. As with other beta2-agonists, special caution should be observed when using Proventil HFA Inhalation Aerosol in elderly patients who have concomitant cardiovascular disease that could be adversely affected by this class of drug.



Adverse Reactions


Adverse reaction information concerning PROVENTIL® HFA Inhalation Aerosol is derived from a 12-week, double-blind, double-dummy study which compared Proventil HFA Inhalation Aerosol, a CFC 11/12 propelled albuterol inhaler, and an HFA-134a placebo inhaler in 565 asthmatic patients. The following table lists the incidence of all adverse events (whether considered by the investigator drug related or unrelated to drug) from this study which occurred at a rate of 3% or greater in the Proventil HFA Inhalation Aerosol treatment group and more frequently in the Proventil HFA Inhalation Aerosol treatment group than in the placebo group. Overall, the incidence and nature of the adverse reactions reported for Proventil HFA Inhalation Aerosol and a CFC 11/12 propelled albuterol inhaler were comparable.




















































































Adverse Experience Incidences (% of patients) in a Large 12-week Clinical Trial*
Body System/

Adverse Event (Preferred Term)
PROVENTIL® HFA Inhalation Aerosol (N=193)CFC 11/12 Propelled Albuterol Inhaler (N=186)HFA-134a Placebo Inhaler (N=186)

*This table includes all adverse events (whether considered by the investigator drug related or unrelated to drug) which occurred at an incidence rate of at least 3.0% in the Proventil HFA Inhalation Aerosol group and more frequently in the Proventil HFA Inhalation Aerosol group than in the HFA-134a placebo inhaler group.


Application Site DisordersInhalation Site Sensation692
Inhalation Taste Sensation433
Body as a WholeAllergic Reaction/Symptoms64<1
Back Pain423
Fever625
Central and Peripheral Nervous SystemTremor782
Gastrointestinal SystemNausea1095
Vomiting723
Heart Rate and Rhythm DisorderTachycardia72<1
Psychiatric DisordersNervousness793
Respiratory System DisordersRespiratory Disorder
(unspecified)645
Rhinitis162214
Upper Resp Tract Infection212018
Urinary System DisorderUrinary Tract Infection342

Adverse events reported by less than 3% of the patients receiving Proventil HFA Inhalation Aerosol, and by a greater proportion of Proventil HFA Inhalation Aerosol patients than placebo patients, which have the potential to be related to Proventil HFA Inhalation Aerosol include: dysphonia, increased sweating, dry mouth, chest pain, edema, rigors, ataxia, leg cramps, hyperkinesia, eructation, flatulence, tinnitus, diabetes mellitus, anxiety, depression, somnolence, rash. Palpitation and dizziness have also been observed with Proventil HFA Inhalation Aerosol.


Adverse events reported in a 4-week pediatric clinical trail comparing Proventil HFA Inhalation Aerosol and a CFC 11/12 propelled albuterol inhaler occurred at a low incidence rate and were similar to those seen in the adult trials.


In small, cumulative dose studies, tremor, nervousness, and headache appeared to be dose related.


Rare cases of urticaria, angioedema, rash, bronchospasm, and oropharyngeal edema have been reported after the use of inhaled albuterol. In addition, albuterol, like other sympathomimetic agents, can cause adverse reactions such as hypertension, angina, vertigo, central nervous system stimulation, insomnia, headache, and drying or irritation of the oropharynx.



OVERDOSE


The expected symptoms with overdosage are those of excessive beta-adrenergic stimulation and/or occurrence or exaggeration of any of the symptoms listed under ADVERSE REACTIONS, eg, seizures, angina, hypertension or hypotension, tachycardia with rates up to 200 beats per minute, arrhythmias, nervousness, headache, tremor, dry mouth, palpitation, nausea, dizziness, fatigue, malaise, and insomnia.


Hypokalemia may also occur. As with all sympathomimetic medications, cardiac arrest and even death may be associated with abuse of PROVENTIL® HFA Inhalation Aerosol. Treatment consists of discontinuation of Proventil HFA Inhalation Aerosol together with appropriate symptomatic therapy. The judicious use of a cardioselective beta-receptor blocker may be considered, bearing in mind that such medication can produce bronchospasm. There is insufficient evidence to determine if dialysis is beneficial for overdosage of Proventil HFA Inhalation Aerosol.


The oral median lethal dose of albuterol sulfate in mice is greater than 2000 mg/kg (approximately 6800 times the maximum recommended daily inhalation dose for adults on a mg/m2 basis and approximately 3200 times the maximum recommended daily inhalation dose for children on a mg/m2 basis). In mature rats, the subcutaneous median lethal dose of albuterol sulfate is approximately 450 mg/kg (approximately 3000 times the maximum recommended daily inhalation dose for adults on a mg/m2 basis and approximately 1400 times the maximum recommended daily inhalation dose for children on a mg/m2 basis). In young rats, the subcutaneous median lethal dose is approximately 2000 mg/kg (approximately 14,000 times the maximum recommended daily inhalation dose for adults on a mg/m2 basis and approximately 6400 times the maximum recommended daily inhalation dose for children on a mg/m2 basis). The inhalation median lethal dose has not been determined in animals.



DOSAGE AND ADMINISTRATION


For treatment of acute episodes of bronchospasm or prevention of asthmatic symptoms, the usual dosage for adults and children 4 years of age and older is two inhalations repeated every 4 to 6 hours. More frequent administration or a larger number of inhalations is not recommended. In some patients, one inhalation every 4 hours may be sufficient. Each actuation of PROVENTIL® HFA Inhalation Aerosol delivers 108 mcg of albuterol sulfate (equivalent to 90 mcg of albuterol base) from the mouthpiece. It is recommended to prime the inhaler before using for the first time and in cases where the inhaler has not been used for more than 2 weeks by releasing four “test sprays” into the air, away from the face.



Exercise Induced Bronchospasm Prevention: The usual dosage for adults and children 4 years of age and older is two inhalations 15 to 30 minutes before exercise.


To maintain proper use of this product, it is important that the mouthpiece be washed and dried thoroughly at least once a week. The inhaler may cease to deliver medication if not properly cleaned and dried thoroughly (see PRECAUTIONS, Information for Patients section). Keeping the plastic mouthpiece clean is very important to prevent medication build-up and blockage. The inhaler may cease to deliver medication if not properly cleaned and air dried thoroughly. If the mouthpiece becomes blocked, washing the mouthpiece will remove the blockage.


If a previously effective dose regimen fails to provide the usual response, this may be a marker of destabilization of asthma and requires reevaluation of the patient and the treatment regimen, giving special consideration to the possible need for anti-inflammatory treatment, eg, corticosteroids.



HOW SUPPLIED


PROVENTIL® HFA (albuterol sulfate) Inhalation Aerosol is supplied as a pressurized aluminum canister with a yellow plastic actuator and orange dust cap each in boxes of one. Each actuation delivers 120 mcg of albuterol sulfate from the valve and 108 mcg of albuterol sulfate from the mouthpiece (equivalent to 90 mcg of albuterol base). Canisters with a labeled net weight of 6.7 g contain 200 inhalations (NDC 0085-1132-01).


Rx only. Store between 15°-25°C (59°-77°F). For best results, canister should be at room temperature before use.


SHAKE WELL BEFORE USING.


The yellow actuator supplied with Proventil HFA Inhalation Aerosol should not be used with any other product canister, and actuator from other products should not be used with a Proventil HFA Inhalation Aerosol canister. The correct amount of medication in each canister cannot be assured after 200 actuations, even though the canister is not completely empty. The canister should be discarded when the labeled number of actuations have been used.


WARNING: Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. Exposure to temperatures above 120°F may cause bursting. Keep out of reach of children.


PROVENTI L ® HFA Inhalation Aerosol does not contain chlorfluorocarbons (CFCs) as the propellant.


Developed and Manufactured by

3M Health Care Limited

Loughborough UK


or


3M Drug Delivery Systems

Northridge, CA 91324


for


Schering Corporation,

a subsidiary of

Schering-Plough Corporation,

Kenilworth, NJ 07033 USA


Schering-Plough


© 1996, 1998, Schering Corporation.

All rights reserved.

The trademarks depicted in this piece are owned by their respective companies.


673700

Rev. 02/09



Attention Health Care Professional


Detach Patient's Instructions for Use from package insert and dispense with the product.


PROVENTIL® HFA


(albuterol sulfate)


Inhalation Aerosol


FOR ORAL INHALATION ONLY


Patient's Instructions for Use


Figure 1



Figure 2



Before using your PROVENTIL® HFA (albuterol Sulfate) Inhalation Aerosol, read complete instructions carefully. Children should use Proventil HFA Inhalation Aerosol under adult supervision, as instructed by the patient's doctor


Please note that


  1. SHAKE THE INHALER WELL immediately before each use. Then remove the cap from the mouthpiece (see Figure 1). Check mouthpiece for foreign objects prior to use. Make sure the canister is fully inserted into the actuator.

  2. As with all aerosol medications, it is recommended to prime the inhaler before using for the first time and in cases where the inhaler has not been used for more than 2 weeks. Prime by releasing four “test sprays” into the air, away from your face.

  3. BREATH OUT FULLY THROUGH THE MOUTH, expelling as much air from your lungs as possible. Place the mouthpiece fully into the mouth holding the inhaler in its upright position (see Figure 2) and closing the lips around it.

  4. WHILE BREATHING IN DEEPLY AND SLOWLY THROUGH THE MOUTH, FULLY DEPRESS THE TOP OF THE METAL CANISTER with your index finger (see Figure 2).

  5. HOLD YOUR BREATH AS LONG AS POSSIBLE, up to 10 seconds. Before breathing out, remove the inhaler from your mouth and release your finger from the canister.

  6. If your physician has prescribed additional puffs, wait 1 minute, shake the inhaler again, and repeat steps 3 through 5. Replace the cap after use.

  7. KEEPING THE PLACTIC MOUTHPIECE CLEAN IS EXTREMELY IMPORTANT TO PREVENT MEDICATION BUILD-UP AND BLOCKAGE. THE MOUTHPIECE SHOULD BE WASHED, SHAKEN TO REMOVE EXCESS WATER, AND AIR DRIED THOROUGHLY AT LEAST ONCE A WEEK. INHALER MAY STOP SPRAYING IF NOT PROPERLY CLEANED.
     

    Routine cleaning instructions:

     

    Step 1. To clean, remove the canister and mouthpiece cap. Wash the mouthpiece through the top and bottom with warm running water for 30 seconds at lease once a week (see Figure A). Never immerse the metal canister in water.

    Figure A



     

    Wash mouthpiece under warm running water.

    Figure B



     

    Allow mouthpiece to dry, such as overnight.

    Figure C



     

    When blocked, little or no medicine comes out.

     

    Step 2. To dry, shake off excess water and let the mouthpiece air dry thoroughly, such as overnight (see Figure B). When the mouthpiece is dry, replace the canister and the mouthpiece cap. Blockage from medication buildup is more likely to occur if the mouthpiece is not allowed to air dry thoroughly.

     

    IF YOUR INHALER HAS BECOME BLOCKED (little or no medication coming out of the mouthpiece, see Figure C), wash the mouthpiece as described in Step 1 and air dry thoroughly as described in Step 2.

     

    IF YOU NEED TO USE YOUR INHALER BEFORE IT IS COMPLETELY DRY, SHAKE OFF EXCESS WATER, replace the canister, and test spray twice into the air, away from your face, to remove most of the water remaining in the mouthpiece. Then take your dose as prescribed. After such use, rewash and air dry thoroughly as described in Step 1 and 2.


  8. The correct amount of medication in each inhalation cannot be assured after 200 actuations, even though the canister is not completely empty. The canister should be discarded when the labeled number of actuations have been used. Before you reach the specific number of actuations, you should consult your physician to determine whether a refill is needed. Just as you should not take extra doses without consulting your physician, you also should not stop using Proventil HFA Inhalation Aerosol without consulting your physician.

You may notice a slightly different taste or spray force than you are used to with Proventil HFA Inhalation Aerosol, compared to other albuterol inhalation aerosol products.


DOSAGE:


Use only as directed by your physician.


WARNINGS:


The action of PROVENTIL® HFA Inhalation Aerosol should last up to 4 to 6 hours. Proventil HFA Inhalation Aerosol should not be used more frequently than recommended. Do not increase the number of puffs or frequency of doses of Proventil HFA Inhalation Aerosol without consulting your physician. If you find that treatment with Proventil HFA Inhalation Aerosol becomes less effective for symptomatic relief, your symptoms become worse, and/or you need to use the product more frequently than usual, medical attention should be sought immediately. While you are taking Proventil HFA Inhalation Aerosol, other inhaled drugs should be taken only as directed by your physician. If you are pregnant or nursing, contact your physician about the use of Proventil HFA Inhalation Aerosol.


Common adverse effects of treatment with Proventil HFA Inhalation Aerosol include palpitations, chest pain, rapid heart rate, tremor, or nervousness. Effective and safe use of Proventil HFA Inhalation Aerosol includes an understanding of the way that it should be administered. Use Proventil HFA Inhalation Aerosol only with the yellow actuator supplied with the product. The Proventil HFA Inhalation Aerosol actuator should not be used with other aerosol medications.


For best results, use at room temperature. Avoid exposing product to extreme heat and cold.


Shake well before use.


Contents Under Pressure.


Do not puncture. Do not store near hear or open flame. Exposure to temperatures above 120°F may cause bursting. Never throw container into fire or incinerator. Store between 15° - 25°C (59° - 77°F). Avoid spraying in eyes. Keep out of reach of children.


Further Information: Your PROVENTIL® HFA (albuterol sulfate) Inhalation Aerosol does not contain chlorofluorocarbons (CFCs) as the propellant. Instead, the inhaler contains a hydrofluoroalkane (HFA-134a) as the propellant.


Developed and Manufactured by

3M Health Care Limited

Loughborough UK


or


3M Drug Delivery Systems

Northridge, CA 91324


For Schering Corporation

a subsidiary of

Schering-Plough Corporation,

Kenilworth, NJ 07033 USA


Schering-Plough


Rev. 02/09

673800


© 1996, 1999, Schering Corporation

All rights reserved.


U.S. Patent No. 5,225,183; 5,439,670; 5,605,674; 5,695,743; 5,766,573; and 6,352,684.



Principal Display Panel – USA Canister Label


SCHERING


PROFESSIONAL SAMPLE NOT FOR SALE


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


100 METERED INHALATIONS


NET CONTENTS 3.7g




Principal Display Panel – USA Carton Label


SCHERING


PROFESSIONAL SAMPLE NOT FOR SALE


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


100 METERED INHALATIONS


NET CONTENTS 3.7g


CONTAINS NO


CHLOROFLUOROCARBONS




Principal Display Panel – Ireland Canister Label


PROFESSIONAL SAMPLE NOT FOR SALE


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


100 METERED INHALATIONS


NET CONTENTS 3.7g


Schering-Plough




Principal Display Panel – Ireland Carton Label


SCHERING


PROFESSIONAL SAMPLE NOT FOR SALE


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


100 METERED INHALATIONS


NET CONTENTS 3.7g


CONTAINS NO


CHLOROFLUOROCARBONS


Schering-Plough




Principal Display Panel – USA Canister Label


SCHERING


PROFESSIONAL SAMPLE NOT FOR SALE


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


100 METERED INHALATIONS


NET CONTENTS 3.7g




Principal Display Panel – USA Carton Label


SCHERING


PROFESSIONAL SAMPLE NOT FOR SALE


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


100 METERED INHALATIONS


NET CONTENTS 3.7g


CONTAINS NO


CHLOROFLUOROCARBONS




Principal Display Panel – Ireland Canister Label


SCHERING


PROFESSIONAL SAMPLE NOT FOR SALE


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


100 METERED INHALATIONS


NET CONTENTS 3.7g




Principal Display Panel – Ireland Carton Label


SCHERING


PROFESSIONAL SAMPLE NOT FOR SALE


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


100 METERED INHALATIONS


NET CONTENTS 3.7g


CONTAINS NO


CHLOROFLUOROCARBONS




Principal Display Panel – USA Canister Label


SCHERING


NDC 0085-1132-01


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


200 METERED INHALATIONS


NET CONTENTS 6.7g


Manufactured for Schering Corporation


Kenilworth, NJ 07033




Principal Display Panel – USA Carton Label


SCHERING


NDC 0085-1132-01


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


200 METERED INHALATIONS


NET CONTENTS 6.7g


CONTAINS NO


CHLOROFLUOROCARBONS




Principal Display Panel – Ireland Canister Label


NDC 0085-1132-01


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


200 METERED INHALATIONS


NET CONTENTS 6.7g


Mfd. for Schering Corp, a subsidiary


of Schering-Plough Corp.


Kenilworth, NJ 07033 USA


Schering-Plough




Principal Display Panel – Ireland Carton Label


NDC 0085-1132-01


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


200 METERED INHALATIONS


NET CONTENTS 6.7g


CONTAINS NO


CHLOROFLUOROCARBONS


Schering-Plough




Principal Display Panel – USA Canister Label


SCHERING


NDC 0085-1132-01