Does ISOSORBIDE MONONITRATE Cause Product prescribing error? 22 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Product prescribing error have been filed in association with ISOSORBIDE MONONITRATE (Isosorbide Mononitrate). This represents 0.9% of all adverse event reports for ISOSORBIDE MONONITRATE.
22
Reports of Product prescribing error with ISOSORBIDE MONONITRATE
0.9%
of all ISOSORBIDE MONONITRATE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Product prescribing error From ISOSORBIDE MONONITRATE?
Of the 22 reports, 5 (22.7%) required hospitalization.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ISOSORBIDE MONONITRATE. However, 22 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 Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which ISOSORBIDE MONONITRATE Alternatives Have Lower Product prescribing error Risk?
ISOSORBIDE MONONITRATE vs ISOTRETINOIN
ISOSORBIDE MONONITRATE vs ISRADIPINE
ISOSORBIDE MONONITRATE vs ISTRADEFYLLINE
ISOSORBIDE MONONITRATE vs ITACITINIB
ISOSORBIDE MONONITRATE vs ITRACONAZOLE