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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 AMINOSALICYLATE Cause Maternal exposure timing unspecified? 17 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Maternal exposure timing unspecified have been filed in association with AMINOSALICYLATE. This represents 6.3% of all adverse event reports for AMINOSALICYLATE.

17
Reports of Maternal exposure timing unspecified with AMINOSALICYLATE
6.3%
of all AMINOSALICYLATE reports
17
Deaths
17
Hospitalizations

How Dangerous Is Maternal exposure timing unspecified From AMINOSALICYLATE?

Of the 17 reports, 17 (100.0%) resulted in death, 17 (100.0%) required hospitalization, and 17 (100.0%) were considered life-threatening.

Is Maternal exposure timing unspecified Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AMINOSALICYLATE. However, 17 reports have been filed with the FAERS database.

What Other Side Effects Does AMINOSALICYLATE Cause?

Vomiting (146) Type 2 diabetes mellitus (138) Abdominal discomfort (121) Mobility decreased (120) Decreased appetite (118) Infusion related reaction (117) Dizziness (116) Hypertension (116) Hypoaesthesia (116) Fatigue (115)

What Other Drugs Cause Maternal exposure timing unspecified?

RITUXIMAB (402) METHOTREXATE (350) ADALIMUMAB (343) DICLOFENAC (331) TOCILIZUMAB (327) HYDROXYCHLOROQUINE (309) FOLIC ACID (304) INFLIXIMAB (303) LEFLUNOMIDE (302) SECUKINUMAB (301)

Which AMINOSALICYLATE Alternatives Have Lower Maternal exposure timing unspecified Risk?

AMINOSALICYLATE vs AMINOSALICYLIC ACID AMINOSALICYLATE vs AMIODARONE AMINOSALICYLATE vs AMISULPRIDE AMINOSALICYLATE vs AMITRIPTYLINE AMINOSALICYLATE vs AMITRIPTYLINE\PERPHENAZINE

Related Pages

AMINOSALICYLATE Full Profile All Maternal exposure timing unspecified Reports All Drugs Causing Maternal exposure timing unspecified AMINOSALICYLATE Demographics