Does PROPRANOLOL Cause Product dose omission? 36 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Product dose omission have been filed in association with PROPRANOLOL (Propranolol Hydrochloride). This represents 0.2% of all adverse event reports for PROPRANOLOL.
36
Reports of Product dose omission with PROPRANOLOL
0.2%
of all PROPRANOLOL reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product dose omission From PROPRANOLOL?
Of the 36 reports, 3 (8.3%) required hospitalization, and 1 (2.8%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PROPRANOLOL. However, 36 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?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which PROPRANOLOL Alternatives Have Lower Product dose omission Risk?
PROPRANOLOL vs PROPRANOLOL\PROPRANOLOL
PROPRANOLOL vs PROPYLENE GLYCOL
PROPRANOLOL vs PROPYLTHIOURACIL
PROPRANOLOL vs PROTAMINE
PROPRANOLOL vs PROTHIPENDYL