Does HYDROXOCOBALAMIN Cause Incorrect product administration duration? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Incorrect product administration duration have been filed in association with HYDROXOCOBALAMIN (Cyanokit). This represents 1.8% of all adverse event reports for HYDROXOCOBALAMIN.
9
Reports of Incorrect product administration duration with HYDROXOCOBALAMIN
1.8%
of all HYDROXOCOBALAMIN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Incorrect product administration duration From HYDROXOCOBALAMIN?
Of the 9 reports, 1 (11.1%) 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 HYDROXOCOBALAMIN. However, 9 reports have been filed with the FAERS database.
What Other Side Effects Does HYDROXOCOBALAMIN Cause?
Acute kidney injury (64)
Somnolence (62)
Coma (59)
Product use in unapproved indication (57)
Gastrooesophageal reflux disease (50)
Pneumonia aspiration (50)
Chromaturia (48)
Off label use (42)
Drug ineffective (41)
Underdose (26)
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 HYDROXOCOBALAMIN Alternatives Have Lower Incorrect product administration duration Risk?
HYDROXOCOBALAMIN vs HYDROXYCHLOROQUINE
HYDROXOCOBALAMIN vs HYDROXYCHLOROQUINE DIPHOSPHATE
HYDROXOCOBALAMIN vs HYDROXYETHYL STARCH 130/0.4
HYDROXOCOBALAMIN vs HYDROXYPROGESTERONE
HYDROXOCOBALAMIN vs HYDROXYPROGESTERONE CAPROATE