Does CLONIDINE Cause Incorrect product administration duration? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Incorrect product administration duration have been filed in association with CLONIDINE (Clonidine hydrochloride). This represents 0.1% of all adverse event reports for CLONIDINE.
8
Reports of Incorrect product administration duration with CLONIDINE
0.1%
of all CLONIDINE reports
3
Deaths
4
Hospitalizations
How Dangerous Is Incorrect product administration duration From CLONIDINE?
Of the 8 reports, 3 (37.5%) resulted in death, 4 (50.0%) required hospitalization, and 3 (37.5%) 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 CLONIDINE. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does CLONIDINE Cause?
Drug ineffective (1,899)
Off label use (1,375)
Hypertension (1,164)
Pain (1,077)
Headache (1,031)
Completed suicide (961)
Fatigue (949)
Toxicity to various agents (829)
Overdose (780)
Hypersensitivity (752)
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 CLONIDINE Alternatives Have Lower Incorrect product administration duration Risk?
CLONIDINE vs CLOPIDOGREL
CLONIDINE vs CLOPIDOGREL BESILATE
CLONIDINE vs CLOPIDOGREL BISULFATE
CLONIDINE vs CLORAZEPATE
CLONIDINE vs CLOSTRIDIUM TETANI TOXOID ANTIGEN