Does TIZANIDINE Cause Product administration interrupted? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product administration interrupted have been filed in association with TIZANIDINE (Tizanidne hydrochloride). This represents 0.2% of all adverse event reports for TIZANIDINE.
13
Reports of Product administration interrupted with TIZANIDINE
0.2%
of all TIZANIDINE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product administration interrupted From TIZANIDINE?
Of the 13 reports, 3 (23.1%) required hospitalization.
Is Product administration interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TIZANIDINE. However, 13 reports have been filed with the FAERS database.
What Other Side Effects Does TIZANIDINE Cause?
Somnolence (631)
Completed suicide (619)
Drug ineffective (510)
Toxicity to various agents (409)
Coma (348)
Fall (334)
Fatigue (330)
Gastrooesophageal reflux disease (324)
Pneumonia aspiration (324)
Dizziness (308)
What Other Drugs Cause Product administration interrupted?
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446)
SODIUM OXYBATE (1,272)
CANNABIDIOL (511)
ISOTRETINOIN (503)
APREMILAST (314)
TREPROSTINIL (295)
EPOPROSTENOL (205)
LENALIDOMIDE (146)
ETANERCEPT (142)
INTERFERON BETA-1A (115)
Which TIZANIDINE Alternatives Have Lower Product administration interrupted Risk?
TIZANIDINE vs TOBACCO LEAF
TIZANIDINE vs TOBI
TIZANIDINE vs TOBI PODHALER
TIZANIDINE vs TOBRAMYCIN
TIZANIDINE vs TOBRAMYCIN\TOBRAMYCIN