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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 Haemoglobin decreased? 155 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 155 reports of Haemoglobin decreased have been filed in association with TADALAFIL (Esokalli Testosterone Booster Oral Dissolving Film). This represents 0.5% of all adverse event reports for TADALAFIL.

155
Reports of Haemoglobin decreased with TADALAFIL
0.5%
of all TADALAFIL reports
25
Deaths
105
Hospitalizations

How Dangerous Is Haemoglobin decreased From TADALAFIL?

Of the 155 reports, 25 (16.1%) resulted in death, 105 (67.7%) required hospitalization, and 13 (8.4%) were considered life-threatening.

Is Haemoglobin decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TADALAFIL. However, 155 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 Haemoglobin decreased?

LENALIDOMIDE (4,031) RUXOLITINIB (3,297) ECULIZUMAB (3,028) ADALIMUMAB (2,459) CLOZAPINE (2,396) RITUXIMAB (1,803) APIXABAN (1,779) NIRAPARIB (1,759) METHOTREXATE (1,754) RIBAVIRIN (1,753)

Which TADALAFIL Alternatives Have Lower Haemoglobin decreased Risk?

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

Related Pages

TADALAFIL Full Profile All Haemoglobin decreased Reports All Drugs Causing Haemoglobin decreased TADALAFIL Demographics