AlleRx Dose Pack Side Effects
Generic name: chlorpheniramine / methscopolamine / phenylephrine / pseudoephedrine
Note: This document provides detailed information about AlleRx Dose Pack.
Applies to chlorpheniramine/methscopolamine/phenylephrine/pseudoephedrine: oral kit Side Effects associated with chlorpheniramine / methscopolamine / phenylephrine / pseudoephedrine. Some dosage forms listed on this page may not apply specifically to the brand name AlleRx Dose Pack.
Applies to chlorpheniramine/methscopolamine/phenylephrine/pseudoephedrine: oral kit.
Cardiovascular adverse events
Cardiovascular side effects have included tachycardia, palpitations, flushing, arrhythmias, and cardiovascular collapse with hypotension.[Ref]
Nervous system
Nervous system side effects have included lassitude, drowsiness, giddiness, increased irritability or excitement, headache, fear, anxiety, nervousness,dizziness, restlessness, tremor, weakness, insomnia, hallucinations, convulsions, and CNS depression.[Ref]
Ocular
Ocular side effects have included blurred vision.[Ref]
Gastrointestinal
Gastrointestinal side effects have included nausea and excessive dryness of the nose, throat, and mouth.[Ref]
Respiratory
Respiratory side effects have included respiratory difficulty.[Ref]
Genitourinary
Genitourinary side effects have included dysuria and urinary retention in patients with prostatic hypertrophy.[Ref]
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References
1. "Product Information. AlleRx Dose Pack (chlorpheniramine/methscopolamine/PE/PSE)." Cornerstone Therapeutics
More about AlleRx Dose Pack (chlorpheniramine / methscopolamine / phenylephrine / pseudoephedrine)
- Check interactions
- Compare alternatives
- Dosage information
- During pregnancy
- Drug class: upper respiratory combinations
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Further information
AlleRx Dose Pack side effects can vary depending on the individual. Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
Note: Medication side effects may be underreported. If you are experiencing side effects that are not listed, submit a report to the FDA by following this guide.