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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 ACRIVASTINE Cause Product use issue? 14 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product use issue have been filed in association with ACRIVASTINE. This represents 16.9% of all adverse event reports for ACRIVASTINE.

14
Reports of Product use issue with ACRIVASTINE
16.9%
of all ACRIVASTINE reports
0
Deaths
7
Hospitalizations

How Dangerous Is Product use issue From ACRIVASTINE?

Of the 14 reports, 7 (50.0%) required hospitalization.

Is Product use issue Listed in the Official Label?

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

What Other Side Effects Does ACRIVASTINE Cause?

Pain (30) Drug hypersensitivity (29) Off label use (27) Somnolence (27) Fatigue (26) Drug ineffective (25) Infection (23) Pruritus (21) Dyspnoea (20) Drug intolerance (19)

What Other Drugs Cause Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Related Pages

ACRIVASTINE Full Profile All Product use issue Reports All Drugs Causing Product use issue ACRIVASTINE Demographics