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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 SITAGLIPTIN Cause Haemoglobin decreased? 32 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 32 reports of Haemoglobin decreased have been filed in association with SITAGLIPTIN (JANUVIA). This represents 0.2% of all adverse event reports for SITAGLIPTIN.

32
Reports of Haemoglobin decreased with SITAGLIPTIN
0.2%
of all SITAGLIPTIN reports
15
Deaths
22
Hospitalizations

How Dangerous Is Haemoglobin decreased From SITAGLIPTIN?

Of the 32 reports, 15 (46.9%) resulted in death, 22 (68.8%) required hospitalization, and 2 (6.3%) 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 SITAGLIPTIN. However, 32 reports have been filed with the FAERS database.

What Other Side Effects Does SITAGLIPTIN Cause?

Blood glucose increased (1,427) Pancreatic carcinoma (1,142) Product dose omission issue (1,125) Drug ineffective (1,057) No adverse event (994) Nausea (936) Pancreatitis (922) Diabetes mellitus inadequate control (744) Diarrhoea (712) Hypoglycaemia (674)

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 SITAGLIPTIN Alternatives Have Lower Haemoglobin decreased Risk?

SITAGLIPTIN vs SOAP SITAGLIPTIN vs SODIUM SITAGLIPTIN vs SODIUM BICARBONATE SITAGLIPTIN vs SODIUM BICARBONATE\SODIUM SITAGLIPTIN vs SODIUM BORATE

Related Pages

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