Drug Safety Information for BROMFED-DM (Brompheniramine maleate; dextromethorphan hydrobromide; pseudoephedrine hydrochloride)

Number of FDA Adverse Event Reports by Patient Age for BROMFED-DM

Total Reports Filed with FDA: 1990*

* Reports for drugs with the same active ingredients have been aggregated in this analysis: Brompheniramine maleate; dextromethorphan hydrobromide; pseudoephedrine hydrochloride (Dimetane-dx, Bromfed-dm, Bromanate dm, Neo, Bio dtuss, Brom/pse/dm, Brovex psb dm, Endacof pd, Lohist psb dm, Q-tapp dm elixir, Bromfeddm, Bromfed)

Charts are based on 1990 reports filed with the FDA between 2004 and June 2015.

Adverse Event Reports are submitted to the FDA by pharmaceutical companies (mandatory reporting is required by manufacturers, distributors, or importers), health care providers such as doctors (voluntary reporting), and by patients themselves (voluntary reporting). More Information on FDA MedWatch (FDA Safety Information and Adverse Event Reporting Program)Voluntary reporting takes place under the FDA's MedWatch program, where health care professionals and consumers submit reports to FDA when they find a problem with a drug, medical device, biologic, or other FDA-regulated product. An adverse event is any undesirable experience or extreme side effect associated with the use of a medical product. Adverse events include: death, life threatening event, hospitalization, disability or permanent damage, congenital anomaly or birth defect, medical product use requiring a surgical or other intervention, or other serious medical situation believed to be caused by the drug.