Does OXAZEPAM Cause Incorrect product administration duration? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Incorrect product administration duration have been filed in association with OXAZEPAM (Oxazepam). This represents 0.1% of all adverse event reports for OXAZEPAM.
18
Reports of Incorrect product administration duration with OXAZEPAM
0.1%
of all OXAZEPAM reports
0
Deaths
1
Hospitalizations
How Dangerous Is Incorrect product administration duration From OXAZEPAM?
Of the 18 reports, 1 (5.6%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OXAZEPAM. However, 18 reports have been filed with the FAERS database.
What Other Side Effects Does OXAZEPAM Cause?
Toxicity to various agents (2,637)
Drug abuse (1,464)
Fall (1,344)
Coma (1,256)
Hypotension (1,188)
Somnolence (962)
Depressed level of consciousness (924)
Intentional overdose (895)
Orthostatic hypotension (714)
Sedation (709)
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 OXAZEPAM Alternatives Have Lower Incorrect product administration duration Risk?
OXAZEPAM vs OXCARBAZEPINE
OXAZEPAM vs OXITRIPTAN
OXAZEPAM vs OXOMEMAZINE
OXAZEPAM vs OXY TAB
OXAZEPAM vs OXYBATE