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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 FAMOTIDINE Cause Condition aggravated? 185 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 185 reports of Condition aggravated have been filed in association with FAMOTIDINE (FAMOTIDINE). This represents 2.2% of all adverse event reports for FAMOTIDINE.

185
Reports of Condition aggravated with FAMOTIDINE
2.2%
of all FAMOTIDINE reports
5
Deaths
53
Hospitalizations

How Dangerous Is Condition aggravated From FAMOTIDINE?

Of the 185 reports, 5 (2.7%) resulted in death, 53 (28.6%) required hospitalization, and 17 (9.2%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

Yes, Condition aggravated is listed as a known adverse reaction in the official FDA drug label for FAMOTIDINE.

What Other Side Effects Does FAMOTIDINE Cause?

Drug ineffective (1,656) Off label use (714) Product use in unapproved indication (553) Nausea (323) Exposure during pregnancy (317) Diarrhoea (315) Dizziness (310) Therapeutic response unexpected (287) Fatigue (241) Headache (233)

What Other Drugs Cause Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which FAMOTIDINE Alternatives Have Lower Condition aggravated Risk?

FAMOTIDINE vs FAMOTIDINE\IBUPROFEN FAMOTIDINE vs FARICIMAB FAMOTIDINE vs FARICIMAB-SVOA FAMOTIDINE vs FARICIMAB\FARICIMAB-SVOA FAMOTIDINE vs FASLODEX

Related Pages

FAMOTIDINE Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated FAMOTIDINE Demographics