Does FOSPHENYTOIN Cause Wrong product administered? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Wrong product administered have been filed in association with FOSPHENYTOIN (CEREBYX). This represents 0.4% of all adverse event reports for FOSPHENYTOIN.
6
Reports of Wrong product administered with FOSPHENYTOIN
0.4%
of all FOSPHENYTOIN reports
1
Deaths
3
Hospitalizations
How Dangerous Is Wrong product administered From FOSPHENYTOIN?
Of the 6 reports, 1 (16.7%) resulted in death, 3 (50.0%) required hospitalization, and 1 (16.7%) were considered life-threatening.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FOSPHENYTOIN. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does FOSPHENYTOIN Cause?
Drug ineffective (406)
Off label use (164)
Status epilepticus (82)
Multiple-drug resistance (77)
Cardiac arrest (72)
Seizure (70)
Drug ineffective for unapproved indication (63)
Hypotension (56)
Toxicity to various agents (53)
Bradycardia (39)
What Other Drugs Cause Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which FOSPHENYTOIN Alternatives Have Lower Wrong product administered Risk?
FOSPHENYTOIN vs FOSTAMATINIB
FOSPHENYTOIN vs FOSTEMSAVIR TROMETHAMINE
FOSPHENYTOIN vs FOTEMUSTINE
FOSPHENYTOIN vs FRAMYCETIN
FOSPHENYTOIN vs FREMANEZUMAB