Brovex Side Effects
Generic Name: brompheniramine
Note: This page contains information about the side effects of brompheniramine. Some of the dosage forms included on this document may not apply to the brand name Brovex.
Not all side effects for Brovex may be reported. You should always consult a doctor or healthcare professional for medical advice. Side effects can be reported to the FDA here.
For the Consumer
Applies to brompheniramine: 12-hour sustained-release tablets, 24-hour sustained-release capsules
Other dosage forms:
Check with your doctor if any of these most COMMON side effects persist or become bothersome:
Seek medical attention right away if any of these SEVERE side effects occur while taking brompheniramine (the active ingredient contained in Brovex)
Dizziness; drowsiness; dry mouth, throat, and nose; thickening of mucus in nose or throat.
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); fast or irregular heartbeat; fever; mental or mood changes; shortness of breath; sore throat; unusual bleeding or bruising; unusual tiredness or weakness.
For Healthcare Professionals
Applies to brompheniramine: compounding powder, injectable solution, oral capsule, oral capsule extended release, oral liquid, oral suspension extended release, oral tablet, oral tablet chewable extended release, oral tablet extended release
Nervous system side effects have included central nervous system (CNS) depression, resulting in drowsiness and sedation in nearly 50% of patients treated. This effect has often been transient and ceased with continued use. Motor skills have be impaired and patients should be advised to avoid tasks which require attention. Patients should also avoid concomitant use with alcohol and other sedative-hypnotic drugs. Dyskinesias have rarely been reported following chronic use of brompheniramine (the active ingredient contained in Brovex)
A few cases of dyskinesias and tremors, often of the face, have been reported in patients whose chronic use of brompheniramine extended over a period of up to 10 years. Some of these cases were only partially relieved by discontinuation of the drug. Haloperidol was successful in relieving symptoms in these patients. Spasmodic torticollis has been reported in a child given brompheniramine over an eight month period.
Gastrointestinal side effects have include nausea, dry mouth and constipation.
Cardiovascular effects of brompheniramine (the active ingredient contained in Brovex) have included hypotension, tachycardia, and palpitations.
Ocular side effects have included blurred vision, diplopia, and dry eyes due to anticholinergic effects.
Genitourinary side effects have included dysuria, urinary hesitancy, decrease in urine flow, and, in rare cases, acute urinary retention.
Hematologic side effects have included rare cases of hemolytic anemia, thrombocytopenia, and agranulocytosis.
More about Brovex (brompheniramine)
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