Does PROPRANOLOL Cause Wrong patient received product? 34 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 34 reports of Wrong patient received product have been filed in association with PROPRANOLOL (Propranolol Hydrochloride). This represents 0.2% of all adverse event reports for PROPRANOLOL.
34
Reports of Wrong patient received product with PROPRANOLOL
0.2%
of all PROPRANOLOL reports
1
Deaths
16
Hospitalizations
How Dangerous Is Wrong patient received product From PROPRANOLOL?
Of the 34 reports, 1 (2.9%) resulted in death, 16 (47.1%) required hospitalization, and 12 (35.3%) 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 PROPRANOLOL. However, 34 reports have been filed with the FAERS database.
What Other Side Effects Does PROPRANOLOL Cause?
Off label use (5,157)
Drug ineffective (2,510)
Product use in unapproved indication (2,210)
Product use issue (2,068)
Toxicity to various agents (1,598)
Completed suicide (1,404)
Hypotension (963)
Product administered to patient of inappropriate age (960)
Bradycardia (934)
Nausea (904)
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 PROPRANOLOL Alternatives Have Lower Wrong patient received product Risk?
PROPRANOLOL vs PROPRANOLOL\PROPRANOLOL
PROPRANOLOL vs PROPYLENE GLYCOL
PROPRANOLOL vs PROPYLTHIOURACIL
PROPRANOLOL vs PROTAMINE
PROPRANOLOL vs PROTHIPENDYL