Does PROMETHAZINE Cause Product administration interrupted? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product administration interrupted have been filed in association with PROMETHAZINE (Promethazine Hydrochloride). This represents 0.1% of all adverse event reports for PROMETHAZINE.
8
Reports of Product administration interrupted with PROMETHAZINE
0.1%
of all PROMETHAZINE reports
0
Deaths
4
Hospitalizations
How Dangerous Is Product administration interrupted From PROMETHAZINE?
Of the 8 reports, 4 (50.0%) 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 PROMETHAZINE. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does PROMETHAZINE Cause?
Intentional overdose (3,193)
Intentional self-injury (2,869)
Toxicity to various agents (742)
Tachycardia (653)
Drug hypersensitivity (627)
Fatigue (617)
Depressed level of consciousness (522)
Somnolence (510)
Drug abuse (359)
Akathisia (343)
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 PROMETHAZINE Alternatives Have Lower Product administration interrupted Risk?
PROMETHAZINE vs PROMETHAZINE\PROMETHAZINE
PROMETHAZINE vs PROMETHAZINE\THIOUREA
PROMETHAZINE vs PROPAFENONE
PROMETHAZINE vs PROPARACAINE
PROMETHAZINE vs PROPECIA