Does AREDIA Cause Hepatic lesion? 29 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 29 reports of Hepatic lesion have been filed in association with AREDIA. This represents 17.6% of all adverse event reports for AREDIA.
29
Reports of Hepatic lesion with AREDIA
17.6%
of all AREDIA reports
7
Deaths
19
Hospitalizations
How Dangerous Is Hepatic lesion From AREDIA?
Of the 29 reports, 7 (24.1%) resulted in death, 19 (65.5%) required hospitalization.
Is Hepatic lesion Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AREDIA. However, 29 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 Hepatic lesion?
OCTREOTIDE (296)
EVEROLIMUS (171)
RIBOCICLIB (144)
LETROZOLE (139)
CAPECITABINE (124)
ADALIMUMAB (123)
METHOTREXATE (108)
FULVESTRANT (107)
PALBOCICLIB (104)
CYCLOPHOSPHAMIDE (101)
Which AREDIA Alternatives Have Lower Hepatic lesion Risk?
AREDIA vs ARFORMOTEROL
AREDIA vs ARGATROBAN
AREDIA vs ARGININE
AREDIA vs ARGININE\LYSINE
AREDIA vs ARIMIDEX