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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 PASIREOTIDE Cause Haemoglobin decreased? 22 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Haemoglobin decreased have been filed in association with PASIREOTIDE (Signifor LAR). This represents 1.2% of all adverse event reports for PASIREOTIDE.

22
Reports of Haemoglobin decreased with PASIREOTIDE
1.2%
of all PASIREOTIDE reports
1
Deaths
18
Hospitalizations

How Dangerous Is Haemoglobin decreased From PASIREOTIDE?

Of the 22 reports, 1 (4.5%) resulted in death, 18 (81.8%) required hospitalization.

Is Haemoglobin decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PASIREOTIDE. However, 22 reports have been filed with the FAERS database.

What Other Side Effects Does PASIREOTIDE Cause?

Hyperglycaemia (252) Diabetes mellitus (224) Blood glucose increased (219) Diarrhoea (160) Fatigue (160) Nausea (150) Headache (139) Drug ineffective (132) Dizziness (100) Off label use (94)

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 PASIREOTIDE Alternatives Have Lower Haemoglobin decreased Risk?

PASIREOTIDE vs PASIREOTIDE DIASPARTATE PASIREOTIDE vs PATIROMER PASIREOTIDE vs PATISIRAN PASIREOTIDE vs PAXIL PASIREOTIDE vs PAZOPANIB

Related Pages

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