Does ETHYLENEDIAMINE Cause Bone density decreased? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Bone density decreased have been filed in association with ETHYLENEDIAMINE. This represents 31.1% of all adverse event reports for ETHYLENEDIAMINE.
14
Reports of Bone density decreased with ETHYLENEDIAMINE
31.1%
of all ETHYLENEDIAMINE reports
9
Deaths
14
Hospitalizations
How Dangerous Is Bone density decreased From ETHYLENEDIAMINE?
Of the 14 reports, 9 (64.3%) resulted in death, 14 (100.0%) required hospitalization, and 9 (64.3%) were considered life-threatening.
Is Bone density decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ETHYLENEDIAMINE. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does ETHYLENEDIAMINE Cause?
Drug hypersensitivity (37)
Drug ineffective (32)
Drug intolerance (32)
Condition aggravated (31)
Hepatotoxicity (31)
Musculoskeletal stiffness (31)
Pain in extremity (31)
Arthralgia (30)
Infection (30)
Joint swelling (30)
What Other Drugs Cause Bone density decreased?
EMTRICITABINE\TENOFOVIR DISOPROXIL (16,315)
TENOFOVIR DISOPROXIL (10,586)
EFAVIRENZ\EMTRICITABINE\TENOFOVIR DISOPROXIL (9,547)
COBICISTAT\ELVITEGRAVIR\EMTRICITABINE\TENOFOVIR DISOPROXIL (4,529)
EMTRICITABINE\RILPIVIRINE\TENOFOVIR DISOPROXIL (3,497)
TERIPARATIDE (1,178)
DENOSUMAB (968)
METHOTREXATE (599)
ADALIMUMAB (584)
TOCILIZUMAB (573)