Does ALENDRONATE Cause Maternal exposure timing unspecified? 291 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 291 reports of Maternal exposure timing unspecified have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 1.0% of all adverse event reports for ALENDRONATE.
291
Reports of Maternal exposure timing unspecified with ALENDRONATE
1.0%
of all ALENDRONATE reports
193
Deaths
221
Hospitalizations
How Dangerous Is Maternal exposure timing unspecified From ALENDRONATE?
Of the 291 reports, 193 (66.3%) resulted in death, 221 (75.9%) required hospitalization, and 211 (72.5%) 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 ALENDRONATE. However, 291 reports have been filed with the FAERS database.
What Other Side Effects Does ALENDRONATE Cause?
Pain (8,989)
Abdominal discomfort (8,301)
Alopecia (8,286)
Systemic lupus erythematosus (8,139)
Fatigue (8,011)
Rheumatoid arthritis (8,010)
Pemphigus (7,947)
Drug ineffective (7,880)
Glossodynia (7,289)
Swelling (6,458)
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 ALENDRONATE Alternatives Have Lower Maternal exposure timing unspecified Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID