Does ALENDRONIC ACID Cause Incorrect product administration duration? 61 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 61 reports of Incorrect product administration duration have been filed in association with ALENDRONIC ACID. This represents 0.8% of all adverse event reports for ALENDRONIC ACID.
61
Reports of Incorrect product administration duration with ALENDRONIC ACID
0.8%
of all ALENDRONIC ACID reports
58
Deaths
59
Hospitalizations
How Dangerous Is Incorrect product administration duration From ALENDRONIC ACID?
Of the 61 reports, 58 (95.1%) resulted in death, 59 (96.7%) required hospitalization, and 58 (95.1%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONIC ACID. However, 61 reports have been filed with the FAERS database.
What Other Side Effects Does ALENDRONIC ACID Cause?
Fatigue (2,540)
Rheumatoid arthritis (2,352)
Pain (2,322)
Glossodynia (2,262)
Alopecia (2,227)
Systemic lupus erythematosus (2,225)
Rash (2,221)
Abdominal discomfort (2,208)
Hand deformity (2,150)
Off label use (2,145)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which ALENDRONIC ACID Alternatives Have Lower Incorrect product administration duration Risk?
ALENDRONIC ACID vs ALEVE
ALENDRONIC ACID vs ALEVE CAPLET
ALENDRONIC ACID vs ALEVE LIQUID
ALENDRONIC ACID vs ALFACALCIDOL
ALENDRONIC ACID vs ALFENTANIL