Does ISOSORBIDE MONONITRATE Cause Wrong patient received product? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Wrong patient received product have been filed in association with ISOSORBIDE MONONITRATE (Isosorbide Mononitrate). This represents 0.4% of all adverse event reports for ISOSORBIDE MONONITRATE.
11
Reports of Wrong patient received product with ISOSORBIDE MONONITRATE
0.4%
of all ISOSORBIDE MONONITRATE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Wrong patient received product From ISOSORBIDE MONONITRATE?
Of the 11 reports.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ISOSORBIDE MONONITRATE. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does ISOSORBIDE MONONITRATE Cause?
Dizziness (554)
Headache (500)
Dyspnoea (462)
Chest pain (458)
Nausea (458)
Fatigue (446)
Diarrhoea (439)
Pruritus (416)
Myocardial infarction (409)
Malaise (405)
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 ISOSORBIDE MONONITRATE Alternatives Have Lower Wrong patient received product Risk?
ISOSORBIDE MONONITRATE vs ISOTRETINOIN
ISOSORBIDE MONONITRATE vs ISRADIPINE
ISOSORBIDE MONONITRATE vs ISTRADEFYLLINE
ISOSORBIDE MONONITRATE vs ITACITINIB
ISOSORBIDE MONONITRATE vs ITRACONAZOLE