Does MINOCYCLINE Cause Incorrect product administration duration? 62 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 62 reports of Incorrect product administration duration have been filed in association with MINOCYCLINE (Minocycline Hydrochloride). This represents 0.9% of all adverse event reports for MINOCYCLINE.
62
Reports of Incorrect product administration duration with MINOCYCLINE
0.9%
of all MINOCYCLINE reports
60
Deaths
60
Hospitalizations
How Dangerous Is Incorrect product administration duration From MINOCYCLINE?
Of the 62 reports, 60 (96.8%) resulted in death, 60 (96.8%) required hospitalization, and 59 (95.2%) 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 MINOCYCLINE. However, 62 reports have been filed with the FAERS database.
What Other Side Effects Does MINOCYCLINE Cause?
Drug ineffective (1,922)
Off label use (1,514)
Drug intolerance (1,190)
Rheumatoid arthritis (1,168)
Pain (1,056)
Drug hypersensitivity (1,012)
Nausea (994)
Arthralgia (948)
Joint swelling (927)
Rash (897)
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 MINOCYCLINE Alternatives Have Lower Incorrect product administration duration Risk?
MINOCYCLINE vs MINOCYCLINE\MINOCYCLINE
MINOCYCLINE vs MINODRONIC ACID
MINOCYCLINE vs MINOXIDIL
MINOCYCLINE vs MIPOMERSEN
MINOCYCLINE vs MIRABEGRON