Does CLONIDINE Cause Product dose omission issue? 63 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 63 reports of Product dose omission issue have been filed in association with CLONIDINE (Clonidine hydrochloride). This represents 0.5% of all adverse event reports for CLONIDINE.
63
Reports of Product dose omission issue with CLONIDINE
0.5%
of all CLONIDINE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product dose omission issue From CLONIDINE?
Of the 63 reports, 2 (3.2%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CLONIDINE. However, 63 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 Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which CLONIDINE Alternatives Have Lower Product dose omission issue Risk?
CLONIDINE vs CLOPIDOGREL
CLONIDINE vs CLOPIDOGREL BESILATE
CLONIDINE vs CLOPIDOGREL BISULFATE
CLONIDINE vs CLORAZEPATE
CLONIDINE vs CLOSTRIDIUM TETANI TOXOID ANTIGEN