Does ALENDRONATE Cause Excessive granulation tissue? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Excessive granulation tissue have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 0.0% of all adverse event reports for ALENDRONATE.
5
Reports of Excessive granulation tissue with ALENDRONATE
0.0%
of all ALENDRONATE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Excessive granulation tissue From ALENDRONATE?
Of the 5 reports, 1 (20.0%) required hospitalization.
Is Excessive granulation tissue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 5 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 Excessive granulation tissue?
CARBIDOPA\LEVODOPA (117)
ADALIMUMAB (38)
BACLOFEN (31)
ZOLEDRONIC ACID (29)
ZOMETA (27)
AREDIA (21)
METHOTREXATE (19)
RITUXIMAB (13)
BECAPLERMIN (11)
PAMIDRONATE (11)
Which ALENDRONATE Alternatives Have Lower Excessive granulation tissue Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID