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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 PARITAPREVIR Cause Haemoglobin decreased? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Haemoglobin decreased have been filed in association with PARITAPREVIR. This represents 4.0% of all adverse event reports for PARITAPREVIR.

8
Reports of Haemoglobin decreased with PARITAPREVIR
4.0%
of all PARITAPREVIR reports
2
Deaths
0
Hospitalizations

How Dangerous Is Haemoglobin decreased From PARITAPREVIR?

Of the 8 reports, 2 (25.0%) resulted in death, and 1 (12.5%) 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 PARITAPREVIR. However, 8 reports have been filed with the FAERS database.

What Other Side Effects Does PARITAPREVIR Cause?

Anaemia (32) Fatigue (32) Hyperbilirubinaemia (25) Headache (19) Insomnia (19) Drug interaction (17) Alanine aminotransferase increased (16) Hepatic failure (16) Nausea (16) Hepatocellular carcinoma (15)

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 PARITAPREVIR Alternatives Have Lower Haemoglobin decreased Risk?

PARITAPREVIR vs PAROXETINE PARITAPREVIR vs PAROXETINE\PAROXETINE PARITAPREVIR vs PAROXETINE\PAROXETINE ANHYDROUS PARITAPREVIR vs PASIREOTIDE PARITAPREVIR vs PASIREOTIDE DIASPARTATE

Related Pages

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