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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 Product substitution issue? 190 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 190 reports of Product substitution issue have been filed in association with TADALAFIL (Esokalli Testosterone Booster Oral Dissolving Film). This represents 0.6% of all adverse event reports for TADALAFIL.

190
Reports of Product substitution issue with TADALAFIL
0.6%
of all TADALAFIL reports
0
Deaths
11
Hospitalizations

How Dangerous Is Product substitution issue From TADALAFIL?

Of the 190 reports, 11 (5.8%) required hospitalization.

Is Product substitution issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TADALAFIL. However, 190 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 Product substitution issue?

AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (2,832) BUPROPION (1,578) METHYLPHENIDATE (1,408) CLONAZEPAM (1,288) LAMOTRIGINE (979) ALBUTEROL (864) LEVOTHYROXINE (803) DULOXETINE (766) ESTRADIOL (692) SERTRALINE (636)

Which TADALAFIL Alternatives Have Lower Product substitution issue Risk?

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

Related Pages

TADALAFIL Full Profile All Product substitution issue Reports All Drugs Causing Product substitution issue TADALAFIL Demographics