Does HYDROXOCOBALAMIN Cause Product use in unapproved indication? 57 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 57 reports of Product use in unapproved indication have been filed in association with HYDROXOCOBALAMIN (Cyanokit). This represents 11.4% of all adverse event reports for HYDROXOCOBALAMIN.
57
Reports of Product use in unapproved indication with HYDROXOCOBALAMIN
11.4%
of all HYDROXOCOBALAMIN reports
18
Deaths
5
Hospitalizations
How Dangerous Is Product use in unapproved indication From HYDROXOCOBALAMIN?
Of the 57 reports, 18 (31.6%) resulted in death, 5 (8.8%) required hospitalization, and 2 (3.5%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HYDROXOCOBALAMIN. However, 57 reports have been filed with the FAERS database.
What Other Side Effects Does HYDROXOCOBALAMIN Cause?
Acute kidney injury (64)
Somnolence (62)
Coma (59)
Gastrooesophageal reflux disease (50)
Pneumonia aspiration (50)
Chromaturia (48)
Off label use (42)
Drug ineffective (41)
Underdose (26)
Nausea (25)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which HYDROXOCOBALAMIN Alternatives Have Lower Product use in unapproved indication Risk?
HYDROXOCOBALAMIN vs HYDROXYCHLOROQUINE
HYDROXOCOBALAMIN vs HYDROXYCHLOROQUINE DIPHOSPHATE
HYDROXOCOBALAMIN vs HYDROXYETHYL STARCH 130/0.4
HYDROXOCOBALAMIN vs HYDROXYPROGESTERONE
HYDROXOCOBALAMIN vs HYDROXYPROGESTERONE CAPROATE