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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does BROMHEXINE Cause Intentional product use issue? 14 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Intentional product use issue have been filed in association with BROMHEXINE. This represents 5.3% of all adverse event reports for BROMHEXINE.

14
Reports of Intentional product use issue with BROMHEXINE
5.3%
of all BROMHEXINE reports
14
Deaths
4
Hospitalizations

How Dangerous Is Intentional product use issue From BROMHEXINE?

Of the 14 reports, 14 (100.0%) resulted in death, 4 (28.6%) required hospitalization.

Is Intentional product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BROMHEXINE. However, 14 reports have been filed with the FAERS database.

What Other Side Effects Does BROMHEXINE Cause?

Off label use (82) Somnolence (64) Gastrooesophageal reflux disease (55) Coma (54) Pneumonia aspiration (54) Pyrexia (51) Chronic sinusitis (45) Nausea (44) Drug ineffective (42) Underdose (39)

What Other Drugs Cause Intentional product use issue?

INFLIXIMAB (11,028) RITUXIMAB (9,602) INFLIXIMAB-DYYB (7,549) TOCILIZUMAB (5,078) METHOTREXATE (4,087) PREDNISONE (3,961) ABATACEPT (3,693) ADALIMUMAB (3,557) NIVOLUMAB (3,297) LEFLUNOMIDE (3,280)

Which BROMHEXINE Alternatives Have Lower Intentional product use issue Risk?

BROMHEXINE vs BROMOCRIPTINE BROMHEXINE vs BROTIZOLAM BROMHEXINE vs BUCILLAMINE BROMHEXINE vs BUDESONIDE BROMHEXINE vs BUDESONIDE\FORMOTEROL

Related Pages

BROMHEXINE Full Profile All Intentional product use issue Reports All Drugs Causing Intentional product use issue BROMHEXINE Demographics