Tussionex (Hydrocodone and Chlorpheniramine): Side Effects, Uses, Dosage, Interactions, Warnings (2024)

Description for Tussionex

Each 5 mL of TUSSIONEX Pennkinetic Extended-Release Suspension contains hydrocodone polistirex equivalent to 10 mg of hydrocodone bitartrate and chlorpheniramine polistirex equivalent to 8 mg of chlorpheniramine maleate. Hydrocodone is a centrally-acting narcotic antitussive. Chlorpheniramine is an antihistamine. TUSSIONEX Pennkinetic Extended-Release Suspension is for oral use only.

Hydrocodone Polistirex

Sulfonated styrene-divinylbenzene copolymer complex with 4,5α-epoxy-3-methoxy-17- methylmorphinan-6-one.

Chlorpheniramine Polistirex

Sulfonated styrene-divinylbenzene copolymer complex with 2-[p-chloro-α-[2-(dimethylamino)ethyl]- benzyl]pyridine.

Inactive Ingredients

Ascorbic acid, D&C Yellow No. 10, ethylcellulose, FD&C Yellow No. 6, flavor, high fructose corn syrup, methylparaben, polyethylene glycol 3350, polysorbate 80, pregelatinized starch, propylene glycol, propylparaben, purified water, sucrose, vegetable oil, xanthan gum.

Uses for Tussionex

TUSSIONEX Pennkinetic Extended-Release Suspension is indicated for relief of cough and upperrespiratory symptoms associated with allergy or a cold in adults and children 6 years of age and older.

Dosage for Tussionex

It is important that TUSSIONEX is measured with an accurate measuring device (see PRECAUTIONS,PATIENT INFORMATION).

A dosing spoon is provided with the 4 oz (115 mL) packaged product. One side of the spoon is for a 2.5mL dose. The other side of the spoon is for a 5 mL dose. Fill to level the side of the spoon for the dosethat has been prescribed. Do not overfill. Rinse with water after each use.

For prescriptions where a dosing spoon is not provided, a pharmacist can provide an appropriatemeasuring device and can provide instructions for measuring the correct dose. A household teaspoon isnot an accurate measuring device and could lead to overdosage.

Each 5 mL of TUSSIONEX Pennkinetic Extended-Release Suspension contains hydrocodone polistirexequivalent to 10 mg hydrocodone bitartrate, and chlorpheniramine polistirex equivalent to 8 mgchlorpheniramine maleate. Shake well before using. Rinse the measuring device with water after eachuse.

Adults And Children 12 Years And Older

5 mL every 12 hours; do not exceed 10 mL in 24 hours.

Children 6-11 Years Of Age

2.5 mL every 12 hours; do not exceed 5 mL in 24 hours.

This medicine is contraindicated in children under 6 years of age (see CONTRAINDICATIONS).

HOW SUPPLIED

TUSSIONEX Pennkinetic (hydrocodone polistirex and chlorpheniramine polistirex) Extended-ReleaseSuspension, equivalent to 10 mg hydrocodone bitartrate and 8 mg chlorpheniramine maleate per 5 mL, isa gold-colored suspension available as:

• NDC 53014-548-01 4 oz amber plastic bottle containing 115 mL of suspension. Each bottle issupplied with a plastic dosing spoon calibrated for measuring 2.5 mL and 5 mL doses.

For Medical Information

Contact: Medical Affairs Department
Phone: (866) 822-0068
Fax: (770) 970-8859

Storage

Store at 20 to 25° (68 to 77°F); excursions permitted to 15 to 30°C (59 to 86°F) [see USP ControlledRoom Temperature].

Manufactured for: UCB, Inc. Smyrna, GA 30080. Revised: Jan 2017

Side Effects for Tussionex

Gastrointestinal Disorders

Nausea and vomiting may occur; they are more frequent in ambulatory than in recumbent patients.Prolonged administration of TUSSIONEX Pennkinetic Extended-Release Suspension may produceconstipation.

General Disorders And Administration Site Conditions

Death

Nervous System Disorders

Sedation, drowsiness, mental clouding, lethargy, impairment of mental and physical performance,anxiety, fear, dysphoria, euphoria, dizziness, psychic dependence, mood changes.

Renal And Urinary Disorders

Ureteral spasm, spasm of vesical sphincters, and urinary retention have been reported with opiates.

Respiratory, Thoracic And Mediastinal Disorders

Dryness of the pharynx, occasional tightness of the chest, and respiratory depression (see CONTRAINDICATIONS).

TUSSIONEX Pennkinetic Extended-Release Suspension may produce dose-related respiratorydepression by acting directly on brain stem respiratory centers (see OVERDOSE). Use ofTUSSIONEX Pennkinetic Extended-Release Suspension in children less than 6 years of age has beenassociated with fatal respiratory depression. Overdose with TUSSIONEX Pennkinetic Extended-Release Suspension in children 6 years of age and older, in adolescents, and in adults has beenassociated with fatal respiratory depression.

Skin And Subcutaneous Tissue Disorders

Rash, pruritus.

Drug Interactions for Tussionex

The use of benzodiazepines, opioids, antihistamines, antipsychotics, anti-anxiety agents, or other CNSdepressants (including alcohol) concomitantly with TUSSIONEX Pennkinetic Extended-ReleaseSuspension may cause an additive CNS depressant effect, profound sedation, respiratory depression,coma, and death and should be avoided (see WARNINGS).

The use of MAO inhibitors or tricyclic antidepressants with hydrocodone preparations may increasethe effect of either the antidepressant or hydrocodone.

The concurrent use of other anticholinergics with hydrocodone may produce paralytic ileus.

Drug Abuse And Dependence

TUSSIONEX Pennkinetic Extended-Release Suspension is a Schedule II narcotic. Psychic dependence,physical dependence and tolerance may develop upon repeated administration of narcotics; therefore,TUSSIONEX Pennkinetic Extended-Release Suspension should be prescribed and administered withcaution. However, psychic dependence is unlikely to develop when TUSSIONEX PennkineticExtended-Release Suspension is used for a short time for the treatment of cough. Physical dependence,the condition in which continued administration of the drug is required to prevent the appearance of awithdrawal syndrome, assumes clinically significant proportions only after several weeks of continuedoral narcotic use, although some mild degree of physical dependence may develop after a few days ofnarcotic therapy.

Warnings for Tussionex

Risk From Concomitant Use With Benzodiazepines Or Other CNS Depressants

Concomitant use of opioids, including TUSSIONEX Pennkinetic Extended-Release Suspension, withbenzodiazepines, or other CNS depressants, including alcohol, may result in profound sedation,respiratory depression, coma, and death. Because of these risks, avoid use of opioid cough medicationsin patients taking benzodiazepines, other CNS depressants, or alcohol (see DRUG INTERACTIONS).

Observational studies have demonstrated that concomitant use of opioid analgesics and benzodiazepinesincreases the risk of drug-related mortality compared to use of opioids alone. Because of similarpharmacologic properties, it is reasonable to expect similar risk with concomitant use of opioid coughmedications and benzodiazepines, other CNS depressants, or alcohol.

Advise both patients and caregivers about the risks of respiratory depression and sedation ifTUSSIONEX Pennkinetic Extended-Release Suspension is used with benzodiazepines, alcohol, orother CNS depressants (see PRECAUTIONS, Information For Patients).

Respiratory Depression

As with all narcotics, TUSSIONEX Pennkinetic Extended-Release Suspension produces dose-relatedrespiratory depression by directly acting on brain stem respiratory centers. Hydrocodone affects thecenter that controls respiratory rhythm and may produce irregular and periodic breathing. Cautionshould be exercised when TUSSIONEX Pennkinetic Extended-Release Suspension is usedpostoperatively and in patients with pulmonary disease, or whenever ventilatory function is depressed.If respiratory depression occurs, it may be antagonized by the use of naloxone hydrochloride and othersupportive measures when indicated (see OVERDOSE).

Head Injury And Increased Intracranial Pressure

The respiratory depressant effects of narcotics and their capacity to elevate cerebrospinal fluidpressure may be markedly exaggerated in the presence of head injury, other intracranial lesions, or apre-existing increase in intracranial pressure. Furthermore, narcotics produce adverse reactions, whichmay obscure the clinical course of patients with head injuries.

Acute Abdominal Conditions

The administration of narcotics may obscure the diagnosis or clinical course of patients with acuteabdominal conditions.

Obstructive Bowel Disease

Chronic use of narcotics may result in obstructive bowel disease especially in patients with underlyingintestinal motility disorder.

Pediatric Use

The use of TUSSIONEX Pennkinetic Extended-Release Suspension is contraindicated in children lessthan 6 years of age (see CONTRAINDICATIONS).

In pediatric patients, as well as adults, the respiratory center is sensitive to the depressant action ofnarcotic cough suppressants in a dose-dependent manner. Caution should be exercised whenadministering TUSSIONEX Pennkinetic Extended-Release Suspension to pediatric patients 6 years ofa*ge and older. Overdose or concomitant administration of TUSSIONEX Pennkinetic Extended-ReleaseSuspension with other respiratory depressants may increase the risk of respiratory depression inpediatric patients. Benefit to risk ratio should be carefully considered, especially in pediatric patientswith respiratory embarrassment (e.g., croup) (see PRECAUTIONS).

Precautions for Tussionex

General

Caution is advised when prescribing this drug to patients with narrow-angle glaucoma, asthma, orprostatic hypertrophy.

Special Risk Patients

As with any narcotic agent, TUSSIONEX Pennkinetic Extended-Release Suspension should be usedwith caution in elderly or debilitated patients and those with severe impairment of hepatic or renalfunction, hypothyroidism, Addison's disease, prostatic hypertrophy, or urethral stricture. The usualprecautions should be observed and the possibility of respiratory depression should be kept in mind.

Information For Patients

Advise the patient to read the FDA-approved patient labeling (Medication Guide).

Concomitant Use With Benzodiazepines Or Other CNS Depressants

Inform patients and caregivers that potentially fatal additive effects may occur if TUSSIONEXPennkinetic Extended-Release Suspension is used with benzodiazepines or other CNS depressants,including alcohol. Because of this risk, patients should avoid concomitant use of TUSSIONEXPennkinetic Extended-Release Suspension with benzodiazepines or other CNS depressants, includingalcohol (see WARNINGS and DRUG INTERACTIONS).

Neurological Adverse Reactions

Advise patients that TUSSIONEX Pennkinetic Extended-Release Suspension may produce markeddrowsiness and impair the mental and/or physical abilities required for the performance of potentiallyhazardous tasks such as driving a car or operating machinery. Advise patients to avoid driving oroperating machinery during treatment with TUSSIONEX Pennkinetic Extended-Release Suspension.

Dosing Instructions

Advise patients not to dilute TUSSIONEX Pennkinetic Extended-Release Suspension with other fluidsand not to mix with other drugs as this may alter the resin-binding and change the absorption rate,possibly increasing the toxicity.

Advise patients that TUSSIONEX Pennkinetic Extended-Release Suspension should be measured withan accurate measuring device. A household teaspoon is not an accurate measuring device and could leadto overdosage. A dosing spoon is provided with the 4 oz (115 mL) packaged product. One side of thespoon is for a 2.5 mL dose. The other side of the spoon is for a 5 mL dose. Instruct the patient to fill tolevel the side of the spoon for the dose that has been prescribed. The spoon should not be overfilled.Rinse the measuring device or dosing spoon after each use.

Alternatively, a pharmacist can recommend an appropriate measuring device and can provide instructionsfor measuring the correct dose.

Cough Reflex

Hydrocodone suppresses the cough reflex; as with all narcotics, caution should be exercised whenTUSSIONEX Pennkinetic Extended-Release Suspension is used postoperatively, and in patients withpulmonary disease.

Carcinogenesis, Mutagenesis, Impairment Of Fertility

Carcinogenicity, mutagenicity, and reproductive studies have not been conducted with TUSSIONEXPennkinetic Extended-Release Suspension.

Pregnancy

Teratogenic Effects

Pregnancy Category C

Hydrocodone has been shown to be teratogenic in hamsters when given in doses 700 times the humandose. There are no adequate and well-controlled studies in pregnant women. TUSSIONEX PennkineticExtended-Release Suspension should be used during pregnancy only if the potential benefit justifies thepotential risk to the fetus.

Nonteratogenic Effects

Babies born to mothers who have been taking opioids regularly prior to delivery will be physicallydependent. The withdrawal signs include irritability and excessive crying, tremors, hyperactivereflexes, increased respiratory rate, increased stools, sneezing, yawning, vomiting, and fever. Theintensity of the syndrome does not always correlate with the duration of maternal opioid use or dose.

Labor And Delivery

As with all narcotics, administration of TUSSIONEX Pennkinetic Extended-Release Suspension to themother shortly before delivery may result in some degree of respiratory depression in the newborn,especially if higher doses are used.

Nursing Mothers

It is not known whether this drug is excreted in human milk. Because many drugs are excreted in humanmilk and because of the potential for serious adverse reactions in nursing infants from TUSSIONEXPennkinetic Extended-Release Suspension, a decision should be made whether to discontinue nursing orto discontinue the drug, taking into account the importance of the drug to the mother.

Pediatric Use

The use of TUSSIONEX Pennkinetic Extended-Release Suspension is contraindicated in children lessthan 6 years of age (see CONTRAINDICATIONS and ADVERSE REACTIONS, Respiratory, Thoracic And Mediastinal Disorders).

TUSSIONEX Pennkinetic Extended-Release Suspension should be used with caution in pediatricpatients 6 years of age and older (see WARNINGS, Pediatric Use).

Geriatric Use

Clinical studies of TUSSIONEX did not include sufficient numbers of subjects aged 65 and over todetermine whether they respond differently from younger subjects. Other reported clinical experiencehas not identified differences in responses between the elderly and younger patients. In general, doseselection for an elderly patient should be cautious, usually starting at the low end of the dosing range,reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitantdisease or other drug therapy.

This drug is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drugmay be greater in patients with impaired renal function. Because elderly patients are more likely to havedecreased renal function, care should be taken in dose selection, and it may be useful to monitor renalfunction.

Overdose Information for Tussionex

Signs And Symptoms

Serious overdosage with hydrocodone is characterized by respiratory depression (a decrease inrespiratory rate and/or tidal volume, Cheyne-Stokes respiration, cyanosis), extreme somnolenceprogressing to stupor or coma, skeletal muscle flaccidity, cold and clammy skin, and sometimesbradycardia and hypotension. Although miosis is characteristic of narcotic overdose, mydriasis mayoccur in terminal narcosis or severe hypoxia. In severe overdosage apnea, circulatory collapse, cardiacarrest and death may occur. The manifestations of chlorpheniramine overdosage may vary from centralnervous system depression to stimulation.

Treatment

Primary attention should be given to the reestablishment of adequate respiratory exchange throughprovision of a patent airway and the institution of assisted or controlled ventilation. The narcoticantagonist naloxone hydrochloride is a specific antidote for respiratory depression which may resultfrom overdosage or unusual sensitivity to narcotics including hydrocodone. Therefore, an appropriatedose of naloxone hydrochloride should be administered, preferably by the intravenous route,simultaneously with efforts at respiratory resuscitation. Since the duration of action of hydrocodone inthis formulation may exceed that of the antagonist, the patient should be kept under continuedsurveillance and repeated doses of the antagonist should be administered as needed to maintain adequaterespiration. For further information, see full prescribing information for naloxone hydrochloride. Anantagonist should not be administered in the absence of clinically significant respiratory depression.Oxygen, intravenous fluids, vasopressors and other supportive measures should be employed asindicated. Gastric emptying may be useful in removing unabsorbed drug.

Contraindications for Tussionex

TUSSIONEX Pennkinetic Extended-Release Suspension is contraindicated in patients with a knownallergy or sensitivity to hydrocodone or chlorpheniramine.

The use of TUSSIONEX Pennkinetic Extended-Release Suspension is contraindicated in children lessthan 6 years of age due to the risk of fatal respiratory depression.

Clinical Pharmacology for Tussionex

Hydrocodone is a semisynthetic narcotic antitussive and analgesic with multiple actions qualitativelysimilar to those of codeine. The precise mechanism of action of hydrocodone and other opiates is notknown; however, hydrocodone is believed to act directly on the cough center. In excessive doses,hydrocodone, like other opium derivatives, will depress respiration. The effects of hydrocodone intherapeutic doses on the cardiovascular system are insignificant. Hydrocodone can produce miosis,euphoria, and physical and psychological dependence.

Chlorpheniramine is an antihistamine drug (H₁ receptor antagonist) that also possesses anticholinergicand sedative activity. It prevents released histamine from dilating capillaries and causing edema of therespiratory mucosa.

Hydrocodone release from TUSSIONEX Pennkinetic Extended-Release Suspension is controlled bythe Pennkinetic System, an extended-release drug delivery system, which combines an ion-exchangepolymer matrix with a diffusion rate-limiting permeable coating. Chlorpheniramine release is prolongedby use of an ion-exchange polymer system.

Following multiple dosing with TUSSIONEX Pennkinetic Extended-Release Suspension, hydrocodonemean (S.D.) peak plasma concentrations of 22.8 (5.9) ng/mL occurred at 3.4 hours. Chlorpheniraminemean (S.D.) peak plasma concentrations of 58.4 (14.7) ng/mL occurred at 6.3 hours following multipledosing. Peak plasma levels obtained with an immediate-release syrup occurred at approximately 1.5hours for hydrocodone and 2.8 hours for chlorpheniramine. The plasma half-lives of hydrocodone andchlorpheniramine have been reported to be approximately 4 and 16 hours, respectively.

Patient Information for Tussionex

TUSSIONEX^®
Pennkinetic^®
(tuss-i-necks pen-ki-ne-tik)
(hydrocodone polistirex and chlorpheniramine polistirex) Extended-Release Suspension

What is the most important information I should know about TUSSIONEX PennkineticExtended-Release Suspension?

• Taking TUSSIONEX Pennkinetic Extended-Release Suspension with benzodiazepines, orother central nervous system depressants, including alcohol can cause severe drowsiness,breathing problems (respiratory depression), coma, and death.
• TUSSIONEX Pennkinetic Extended-Release Suspension can cause you to be drowsy. Avoiddriving a car or operating machinery during treatment with TUSSIONEX PennkineticExtended-Release Suspension.
• Women who breastfeed should talk to their healthcare provider before taking TUSSIONEXPennkinetic Extended-Release Suspension.
• Call your healthcare provider or get emergency medical help right away if anyone takingTUSSIONEX Pennkinetic Extended-Release Suspension has any of the symptoms below:
  • increased sleepiness
  • confusion
  • difficulty breathing
  • shallow breathing
  • limpness
  • your baby has difficultybreastfeeding
• Keep TUSSIONEX Pennkinetic Extended-Release Suspension in a safe place away fromchildren. Accidental use by a child is a medical emergency and can cause death. If a childaccidentally takes TUSSIONEX Pennkinetic Extended-Release Suspension, get emergencymedical help right away.
• TUSSIONEX Pennkinetic Extended-Release Suspension can cause serious side effects,TUSSIONEX Pennkinetic Extended-Release Suspension can cause serious side effects,including death.
• Take TUSSIONEX Pennkinetic Extended-Release Suspension exactly as prescribed by yourhealthcare provider. If you take the wrong dose of TUSSIONEX Pennkinetic Extended-Release Suspension, you could overdose and die.
• TUSSIONEX Pennkinetic Extended-Release Suspension is not for children under 6 years ofa*ge.

What is TUSSIONEX Pennkinetic Extended-Release Suspension?

• TUSSIONEX Pennkinetic Extended-Release Suspension is a prescription medicine used totreat cough and upper respiratory symptoms that you can have with allergies or a cold.TUSSIONEX Pennkinetic Extended-Release Suspension is for adults and children age 6 yearsand older. TUSSIONEX Pennkinetic Extended-Release Suspension contains 2 medicines,hydrocodone and chlorpheniramine. Hydrocodone is a narcotic cough suppressant.Chlorpheniramine is an antihistamine.
• TUSSIONEX Pennkinetic Extended-Release Suspension is a federal controlledsubstance (CII) because it contains hydrocodone that can be abused or lead todependence. Keep TUSSIONEX Pennkinetic Extended-Release Suspension in a safe place toprevent misuse and abuse. Selling or giving away TUSSIONEX Pennkinetic Extended-ReleaseSuspension may harm others, and is against the law. Tell your healthcare provider if you haveabused or been dependent on alcohol, prescription medicines or street drugs.
• TUSSIONEX Pennkinetic Extended-Release Suspension is not for children under 6 years ofa*ge.

Who should not take TUSSIONEX Pennkinetic Extended-Release Suspension?

• Do not take TUSSIONEX Pennkinetic Extended-Release Suspension if you are allergic to anyof the ingredients in TUSSIONEX Pennkinetic Extended-Release Suspension. See the end ofthis Medication Guide for a complete list of ingredients. You may have an increased risk ofhaving an allergic reaction to TUSSIONEX Pennkinetic Extended-Release Suspension if youare allergic to certain other opioid medicines.
• Do not give TUSSIONEX Pennkinetic Extended-Release Suspension to a child under 6 yearsof age. It can cause breathing problems that can lead to death.

Before you take TUSSIONEX Pennkinetic Extended-Release Suspension, tell yourhealthcare provider about all of your medical conditions, including if you:

• have a drug dependence
• have lung or breathing problems
• have had a head injury
• have pain in your stomach-area (abdomen)
• have a history of severe or persistent cough
• have glaucoma
• have prostate problems
• have problems with your urinary tract (urethralstricture)
• plan to have surgery
• drink alcohol
• have kidney or liverproblems
• have diabetes
• have thyroid problems, suchas hypothyroidism
• Addison's disease

• are pregnant or plan to become pregnant. It is not known if TUSSIONEX Pennkinetic Extended-Release Suspension will harm your unborn baby. You and your healthcare provider shoulddecide if you should take TUSSIONEX Pennkinetic Extended-Release Suspension while youare pregnant.
• are breastfeeding or plan to breastfeed. It is not known if TUSSIONEX Pennkinetic Extended-Release Suspension passes into your breast milk. You and your healthcare provider shoulddecide if you will take TUSSIONEX Pennkinetic Extended-Release Suspension or breastfeed.You should not do both.

Tell your healthcare provider about all the medicines you take, including prescription andover-the-counter medicines, vitamins, and herbal supplements.

Taking TUSSIONEX Pennkinetic Extended-Release Suspension with certain other medicines cancause side effects or affect how well TUSSIONEX Pennkinetic Extended-Release Suspension orthe other medicines work. Do not start or stop other medicines without talking to your healthcareprovider.

Especially tell your healthcare provider if you:

• take pain medicines such as narcotics
• take cold or allergy medicines that contain antihistamines or cough suppressants
• take medicines for mental illness (anti-psychotics, anti-anxiety)
• drink alcohol
• take medicines for depression, including monoamine oxidase inhibitors (MAOIs) and tricyclics
• take medicines for stomach or intestine problems

Ask your healthcare provider if you are not sure if you take one of these medicines.

How should I take TUSSIONEX Pennkinetic Extended-Release Suspension?

• Take TUSSIONEX Pennkinetic Extended-Release Suspension exactly as your healthcareprovider tells you to take it.
• Your healthcare provider will tell you how much TUSSIONEX Pennkinetic Extended-ReleaseSuspension to take and when to take it. Do not change your dose without talking to yourhealthcare provider.
• Shake TUSSIONEX Pennkinetic Extended-Release Suspension well before each use.
• Do not mix TUSSIONEX Pennkinetic Extended-Release Suspension with other liquids ormedicines. Mixing may change how TUSSIONEX Pennkinetic Extended-Release Suspensionworks.
• TUSSIONEX Pennkinetic Extended-Release Suspension can be taken with or without food.
• Only measure TUSSIONEX Pennkinetic Extended-Release Suspension with the dosingspoon that comes with your prescription. If you do not have a dosing spoon for yourmedicine, ask your pharmacist to give you a measuring device to help you measure the correctamount of TUSSIONEX Pennkinetic Extended-Release Suspension. Do not use a household teaspoon to measure your medicine. You may accidently take too much.
  • One side of the dosing spoon is marked for a 2.5 mL dose. The other side of the spoon ismarked for a 5 mL dose. Find the side of the spoon that has the dose you are taking.
  • Fill that side of the spoon so the medicine is level with the rim of the spoon. Do notoverfill the spoon.
  • Rinse the spoon with water after each use.
• If you take too much TUSSIONEX Pennkinetic Extended-Release Suspension, call yourhealthcare provider or go to the nearest hospital emergency room right away.

What should I avoid while taking TUSSIONEX Pennkinetic Extended-Release Suspension?

• TUSSIONEX Pennkinetic Extended-Release Suspension can cause you to be drowsy. Avoiddriving a car or operating machinery during treatment with TUSSIONEX PennkineticExtended-Release Suspension.
• Avoid drinking alcohol during treatment with TUSSIONEX Pennkinetic Extended-ReleaseSuspension. Drinking alcohol can increase your chances of having serious side effects.

What are the possible side effects of TUSSIONEX Pennkinetic Extended-ReleaseSuspension?

TUSSIONEX Pennkinetic Extended-Release Suspension may cause serious side effects,including:

• See "What is the most important information I should know about TUSSIONEXPennkinetic Extended-Release Suspension?"
• Breathing problems (respiratory depression) which can lead to death. Call yourhealthcare provider or get emergency treatment right away if you are sleeping more than usual,have shallow or slow breathing, or confusion.
• Increased intracranial pressure.
• Physical dependence or abuse. Take TUSSIONEX Pennkinetic Extended-ReleaseSuspension exactly as your healthcare provider tells you to take it. Stopping TUSSIONEXPennkinetic Extended-Release Suspension suddenly can cause withdrawal symptoms.
• Bowel problems including constipation or stomach pain.

The most common side effects of TUSSIONEX Pennkinetic Extended-Release Suspensioninclude:

• sleepiness
• confusion
• nausea and vomiting
• difficulty urinating
• trouble breathing

These are not all the possible side effects of TUSSIONEX Pennkinetic Extended-ReleaseSuspension.

Call your doctor for medical advice about side effects. You may report side effects to FDA at1-800-FDA-1088.

How should I store TUSSIONEX Pennkinetic Extended-Release Suspension?

• Store TUSSIONEX Pennkinetic Extended-Release Suspension at room temperature between68°F to 77°F (20°C to 25°C).
• Safely throw away medicine that is out of date or no longer needed.
• Keep TUSSIONEX Pennkinetic Extended-Release Suspension and all medicines out ofthe reach of children.

General information about the safe and effective use of TUSSIONEX Pennkinetic Extended-Release Suspension.

Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide.Do not use TUSSIONEX Pennkinetic Extended-Release Suspension for a condition for which itwas not prescribed. Do not give TUSSIONEX Pennkinetic Extended-Release Suspension to otherpeople, even if they have the same symptoms that you have. It may harm them.You can ask your pharmacist or healthcare provider for information about TUSSIONEXPennkinetic Extended-Release Suspension that is written for health professionals.

What are the ingredients in TUSSIONEX Pennkinetic Extended-Release Suspension?

Active Ingredient: hydrocodone polistirex and chlorpheniramine polistirex
Inactive Ingredients: Ascorbic acid, D&C Yellow No. 10, ethylcellulose, FD&C Yellow No. 6,flavor, high fructose corn syrup, methylparaben, polyethylene glycol 3350, polysorbate 80,pregelatinized starch, propylene glycol, propylparaben, purified water, sucrose, vegetable oil,xanthan gum.

This Medication Guide has been approved by the U.S.