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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 AREDIA Cause Haemoglobin decreased? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Haemoglobin decreased have been filed in association with AREDIA. This represents 3.6% of all adverse event reports for AREDIA.

6
Reports of Haemoglobin decreased with AREDIA
3.6%
of all AREDIA reports
1
Deaths
4
Hospitalizations

How Dangerous Is Haemoglobin decreased From AREDIA?

Of the 6 reports, 1 (16.7%) resulted in death, 4 (66.7%) required hospitalization.

Is Haemoglobin decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AREDIA. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does AREDIA Cause?

Osteonecrosis of jaw (151) Pain (128) Anxiety (122) Spinal osteoarthritis (114) Osteoarthritis (113) Dyspnoea (107) Arthralgia (102) Osteomyelitis (95) Anaemia (89) Atelectasis (89)

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 AREDIA Alternatives Have Lower Haemoglobin decreased Risk?

AREDIA vs ARFORMOTEROL AREDIA vs ARGATROBAN AREDIA vs ARGININE AREDIA vs ARGININE\LYSINE AREDIA vs ARIMIDEX

Related Pages

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