Does IBANDRONATE Cause Incorrect product administration duration? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Incorrect product administration duration have been filed in association with IBANDRONATE (Ibandronate Sodium). This represents 0.1% of all adverse event reports for IBANDRONATE.
13
Reports of Incorrect product administration duration with IBANDRONATE
0.1%
of all IBANDRONATE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Incorrect product administration duration From IBANDRONATE?
Of the 13 reports, 3 (23.1%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IBANDRONATE. However, 13 reports have been filed with the FAERS database.
What Other Side Effects Does IBANDRONATE Cause?
Femur fracture (990)
Arthralgia (975)
Pain (779)
Pain in extremity (726)
Back pain (688)
Myalgia (623)
Diarrhoea (551)
Low turnover osteopathy (521)
Nausea (480)
Anxiety (456)
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 IBANDRONATE Alternatives Have Lower Incorrect product administration duration Risk?
IBANDRONATE vs IBANDRONIC ACID
IBANDRONATE vs IBERDOMIDE
IBANDRONATE vs IBREXAFUNGERP
IBANDRONATE vs IBRITUMOMAB TIUXETAN
IBANDRONATE vs IBRUTINIB