Does DIETARY SUPPLEMENT Cause Maternal exposure timing unspecified? 34 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 34 reports of Maternal exposure timing unspecified have been filed in association with DIETARY SUPPLEMENT. This represents 1.7% of all adverse event reports for DIETARY SUPPLEMENT.
34
Reports of Maternal exposure timing unspecified with DIETARY SUPPLEMENT
1.7%
of all DIETARY SUPPLEMENT reports
34
Deaths
34
Hospitalizations
How Dangerous Is Maternal exposure timing unspecified From DIETARY SUPPLEMENT?
Of the 34 reports, 34 (100.0%) resulted in death, 34 (100.0%) required hospitalization, and 34 (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 DIETARY SUPPLEMENT. However, 34 reports have been filed with the FAERS database.
What Other Side Effects Does DIETARY SUPPLEMENT Cause?
Off label use (363)
Dyspnoea (357)
Headache (349)
Drug ineffective (347)
Hypertension (328)
Vomiting (322)
Fatigue (312)
Nausea (306)
Condition aggravated (300)
General physical health deterioration (290)
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 DIETARY SUPPLEMENT Alternatives Have Lower Maternal exposure timing unspecified Risk?
DIETARY SUPPLEMENT vs DIETARY SUPPLEMENT\HERBALS
DIETARY SUPPLEMENT vs DIETARY SUPPLEMENT\MINERALS\VITAMINS
DIETARY SUPPLEMENT vs DIETARY SUPPLEMENT\UBIDECARENONE
DIETARY SUPPLEMENT vs DIFELIKEFALIN
DIETARY SUPPLEMENT vs DIFLUNISAL