Does PROPRANOLOL Cause Product dose omission issue? 117 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 117 reports of Product dose omission issue have been filed in association with PROPRANOLOL (Propranolol Hydrochloride). This represents 0.6% of all adverse event reports for PROPRANOLOL.
117
Reports of Product dose omission issue with PROPRANOLOL
0.6%
of all PROPRANOLOL reports
1
Deaths
6
Hospitalizations
How Dangerous Is Product dose omission issue From PROPRANOLOL?
Of the 117 reports, 1 (0.9%) resulted in death, 6 (5.1%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PROPRANOLOL. However, 117 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 Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which PROPRANOLOL Alternatives Have Lower Product dose omission issue Risk?
PROPRANOLOL vs PROPRANOLOL\PROPRANOLOL
PROPRANOLOL vs PROPYLENE GLYCOL
PROPRANOLOL vs PROPYLTHIOURACIL
PROPRANOLOL vs PROTAMINE
PROPRANOLOL vs PROTHIPENDYL