Does MIANSERIN Cause Wrong patient received product? 22 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Wrong patient received product have been filed in association with MIANSERIN. This represents 0.9% of all adverse event reports for MIANSERIN.
22
Reports of Wrong patient received product with MIANSERIN
0.9%
of all MIANSERIN reports
4
Deaths
10
Hospitalizations
How Dangerous Is Wrong patient received product From MIANSERIN?
Of the 22 reports, 4 (18.2%) resulted in death, 10 (45.5%) required hospitalization, and 7 (31.8%) were considered life-threatening.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MIANSERIN. However, 22 reports have been filed with the FAERS database.
What Other Side Effects Does MIANSERIN Cause?
Toxicity to various agents (246)
Fall (201)
Coma (177)
Somnolence (163)
Off label use (141)
Drug abuse (132)
Confusional state (126)
Hyponatraemia (122)
Hypotension (113)
Poisoning deliberate (107)
What Other Drugs Cause Wrong patient received product?
INSULIN LISPRO (334)
CLOZAPINE (198)
RISPERIDONE (176)
OXAZEPAM (152)
BISOPROLOL (150)
LEVETIRACETAM (126)
ACETAMINOPHEN (123)
METFORMIN (116)
INSULIN GLARGINE (114)
CLONAZEPAM (112)
Which MIANSERIN Alternatives Have Lower Wrong patient received product Risk?
MIANSERIN vs MICAFUNGIN
MIANSERIN vs MICARDIS
MIANSERIN vs MICONAZOLE
MIANSERIN vs MIDAZOLAM
MIANSERIN vs MIDAZOLAM\MIDAZOLAM