Does ALENDRONATE\CHOLECALCIFEROL Cause Maternal exposure timing unspecified? 84 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 84 reports of Maternal exposure timing unspecified have been filed in association with ALENDRONATE\CHOLECALCIFEROL. This represents 3.2% of all adverse event reports for ALENDRONATE\CHOLECALCIFEROL.
84
Reports of Maternal exposure timing unspecified with ALENDRONATE\CHOLECALCIFEROL
3.2%
of all ALENDRONATE\CHOLECALCIFEROL reports
76
Deaths
81
Hospitalizations
How Dangerous Is Maternal exposure timing unspecified From ALENDRONATE\CHOLECALCIFEROL?
Of the 84 reports, 76 (90.5%) resulted in death, 81 (96.4%) required hospitalization, and 82 (97.6%) 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\CHOLECALCIFEROL. However, 84 reports have been filed with the FAERS database.
What Other Side Effects Does ALENDRONATE\CHOLECALCIFEROL Cause?
Fatigue (929)
Arthralgia (841)
Hypertension (820)
Depression (747)
Arthropathy (733)
Rash (726)
Alopecia (711)
Abdominal discomfort (705)
Confusional state (696)
Joint swelling (684)
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\CHOLECALCIFEROL Alternatives Have Lower Maternal exposure timing unspecified Risk?
ALENDRONATE\CHOLECALCIFEROL vs ALENDRONIC ACID
ALENDRONATE\CHOLECALCIFEROL vs ALEVE
ALENDRONATE\CHOLECALCIFEROL vs ALEVE CAPLET
ALENDRONATE\CHOLECALCIFEROL vs ALEVE LIQUID
ALENDRONATE\CHOLECALCIFEROL vs ALFACALCIDOL