Does ALENDRONATE Cause Product quality issue? 544 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 544 reports of Product quality issue have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 2.0% of all adverse event reports for ALENDRONATE.
544
Reports of Product quality issue with ALENDRONATE
2.0%
of all ALENDRONATE reports
474
Deaths
421
Hospitalizations
How Dangerous Is Product quality issue From ALENDRONATE?
Of the 544 reports, 474 (87.1%) resulted in death, 421 (77.4%) required hospitalization, and 434 (79.8%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 544 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which ALENDRONATE Alternatives Have Lower Product quality issue Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID