Does ALENDRONATE Cause Product dose omission issue? 194 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 194 reports of Product dose omission issue have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 0.7% of all adverse event reports for ALENDRONATE.
194
Reports of Product dose omission issue with ALENDRONATE
0.7%
of all ALENDRONATE reports
0
Deaths
33
Hospitalizations
How Dangerous Is Product dose omission issue From ALENDRONATE?
Of the 194 reports, 33 (17.0%) required hospitalization, and 9 (4.6%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 194 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 Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which ALENDRONATE Alternatives Have Lower Product dose omission issue Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID