Does PYRIDOSTIGMINE Cause Wrong patient received product? 32 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 32 reports of Wrong patient received product have been filed in association with PYRIDOSTIGMINE (pyridostigmine bromide). This represents 1.6% of all adverse event reports for PYRIDOSTIGMINE.
32
Reports of Wrong patient received product with PYRIDOSTIGMINE
1.6%
of all PYRIDOSTIGMINE reports
0
Deaths
6
Hospitalizations
How Dangerous Is Wrong patient received product From PYRIDOSTIGMINE?
Of the 32 reports, 6 (18.8%) required hospitalization, and 13 (40.6%) 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 PYRIDOSTIGMINE. However, 32 reports have been filed with the FAERS database.
What Other Side Effects Does PYRIDOSTIGMINE Cause?
Drug ineffective (322)
Off label use (238)
Myasthenia gravis (193)
Diarrhoea (167)
Asthenia (129)
Fatigue (110)
Condition aggravated (99)
Nausea (86)
Dyspnoea (85)
Headache (81)
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 PYRIDOSTIGMINE Alternatives Have Lower Wrong patient received product Risk?
PYRIDOSTIGMINE vs PYRIDOXINE
PYRIDOSTIGMINE vs PYRIDOXINE\THIAMINE
PYRIDOSTIGMINE vs PYRIMETHAMINE
PYRIDOSTIGMINE vs PYROTINIB
PYRIDOSTIGMINE vs QSYMIA