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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does CAFFEINE\PHENOBARBITAL Cause Wrong patient received product? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Wrong patient received product have been filed in association with CAFFEINE\PHENOBARBITAL. This represents 10.0% of all adverse event reports for CAFFEINE\PHENOBARBITAL.

6
Reports of Wrong patient received product with CAFFEINE\PHENOBARBITAL
10.0%
of all CAFFEINE\PHENOBARBITAL reports
0
Deaths
6
Hospitalizations

How Dangerous Is Wrong patient received product From CAFFEINE\PHENOBARBITAL?

Of the 6 reports, 6 (100.0%) required hospitalization, and 6 (100.0%) 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 CAFFEINE\PHENOBARBITAL. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does CAFFEINE\PHENOBARBITAL Cause?

Somnolence (9) Accidental overdose (8) Altered state of consciousness (8) Clostridium difficile infection (8) Leukopenia (8) Neutropenia (8) Wrong schedule (6) Foetal exposure during pregnancy (5)

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)

Related Pages

CAFFEINE\PHENOBARBITAL Full Profile All Wrong patient received product Reports All Drugs Causing Wrong patient received product CAFFEINE\PHENOBARBITAL Demographics