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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 TADALAFIL Cause Wrong product administered? 16 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Wrong product administered have been filed in association with TADALAFIL (Esokalli Testosterone Booster Oral Dissolving Film). This represents 0.1% of all adverse event reports for TADALAFIL.

16
Reports of Wrong product administered with TADALAFIL
0.1%
of all TADALAFIL reports
9
Deaths
0
Hospitalizations

How Dangerous Is Wrong product administered From TADALAFIL?

Of the 16 reports, 9 (56.3%) resulted in death.

Is Wrong product administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TADALAFIL. However, 16 reports have been filed with the FAERS database.

What Other Side Effects Does TADALAFIL Cause?

Headache (3,196) Drug ineffective (2,943) Dyspnoea (2,881) Death (1,917) Diarrhoea (1,667) Dizziness (1,374) Nausea (1,368) Asthenia (1,230) Fatigue (1,135) Hypertension (1,044)

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 TADALAFIL Alternatives Have Lower Wrong product administered Risk?

TADALAFIL vs TAFAMIDIS TADALAFIL vs TAFAMIDIS MEGLUMINE TADALAFIL vs TAFASITAMAB TADALAFIL vs TAFASITAMAB-CXIX TADALAFIL vs TAFINLAR

Related Pages

TADALAFIL Full Profile All Wrong product administered Reports All Drugs Causing Wrong product administered TADALAFIL Demographics