Does ALENDRONIC ACID Cause Maternal exposure timing unspecified? 156 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 156 reports of Maternal exposure timing unspecified have been filed in association with ALENDRONIC ACID. This represents 1.9% of all adverse event reports for ALENDRONIC ACID.
156
Reports of Maternal exposure timing unspecified with ALENDRONIC ACID
1.9%
of all ALENDRONIC ACID reports
137
Deaths
153
Hospitalizations
How Dangerous Is Maternal exposure timing unspecified From ALENDRONIC ACID?
Of the 156 reports, 137 (87.8%) resulted in death, 153 (98.1%) required hospitalization, and 153 (98.1%) 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 ALENDRONIC ACID. However, 156 reports have been filed with the FAERS database.
What Other Side Effects Does ALENDRONIC ACID Cause?
Fatigue (2,540)
Rheumatoid arthritis (2,352)
Pain (2,322)
Glossodynia (2,262)
Alopecia (2,227)
Systemic lupus erythematosus (2,225)
Rash (2,221)
Abdominal discomfort (2,208)
Hand deformity (2,150)
Off label use (2,145)
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 ALENDRONIC ACID Alternatives Have Lower Maternal exposure timing unspecified Risk?
ALENDRONIC ACID vs ALEVE
ALENDRONIC ACID vs ALEVE CAPLET
ALENDRONIC ACID vs ALEVE LIQUID
ALENDRONIC ACID vs ALFACALCIDOL
ALENDRONIC ACID vs ALFENTANIL