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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 LATANOPROST Cause Haemoglobin decreased? 59 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 59 reports of Haemoglobin decreased have been filed in association with LATANOPROST (IYUZEH). This represents 0.4% of all adverse event reports for LATANOPROST.

59
Reports of Haemoglobin decreased with LATANOPROST
0.4%
of all LATANOPROST reports
0
Deaths
52
Hospitalizations

How Dangerous Is Haemoglobin decreased From LATANOPROST?

Of the 59 reports, 52 (88.1%) required hospitalization, and 1 (1.7%) 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 LATANOPROST. However, 59 reports have been filed with the FAERS database.

What Other Side Effects Does LATANOPROST Cause?

Treatment failure (5,781) Drug ineffective (1,338) Eye irritation (1,165) Eye pain (668) Hypersensitivity (668) Ocular hyperaemia (587) Intraocular pressure increased (579) Vision blurred (564) Cataract (546) Visual impairment (382)

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 LATANOPROST Alternatives Have Lower Haemoglobin decreased Risk?

LATANOPROST vs LATANOPROSTENE BUNOD LATANOPROST vs LATANOPROST\NETARSUDIL LATANOPROST vs LATANOPROST\TIMOLOL LATANOPROST vs LATISSE LATANOPROST vs LATUDA

Related Pages

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