Does ALENDRONATE Cause Fluid retention? 272 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 272 reports of Fluid retention have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 1.0% of all adverse event reports for ALENDRONATE.
272
Reports of Fluid retention with ALENDRONATE
1.0%
of all ALENDRONATE reports
151
Deaths
210
Hospitalizations
How Dangerous Is Fluid retention From ALENDRONATE?
Of the 272 reports, 151 (55.5%) resulted in death, 210 (77.2%) required hospitalization, and 150 (55.1%) were considered life-threatening.
Is Fluid retention Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 272 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 Fluid retention?
AMBRISENTAN (3,927)
TREPROSTINIL (3,804)
MACITENTAN (2,861)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (2,233)
SACUBITRIL\VALSARTAN (2,187)
ADALIMUMAB (1,193)
SELEXIPAG (1,044)
FUROSEMIDE (1,020)
LENALIDOMIDE (1,007)
EPOPROSTENOL (929)
Which ALENDRONATE Alternatives Have Lower Fluid retention Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID