Does RALTITREXED Cause Condition aggravated? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Condition aggravated have been filed in association with RALTITREXED. This represents 3.3% of all adverse event reports for RALTITREXED.
14
Reports of Condition aggravated with RALTITREXED
3.3%
of all RALTITREXED reports
1
Deaths
8
Hospitalizations
How Dangerous Is Condition aggravated From RALTITREXED?
Of the 14 reports, 1 (7.1%) resulted in death, 8 (57.1%) required hospitalization, and 5 (35.7%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RALTITREXED. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does RALTITREXED Cause?
Diarrhoea (82)
Myelosuppression (77)
Anaemia (49)
Neutropenia (48)
Vomiting (46)
Nausea (45)
Disease progression (40)
Fatigue (38)
Asthenia (33)
Hepatic function abnormal (26)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which RALTITREXED Alternatives Have Lower Condition aggravated Risk?
RALTITREXED vs RAMELTEON
RALTITREXED vs RAMIPRIL
RALTITREXED vs RAMUCIRUMAB
RALTITREXED vs RANEXA
RALTITREXED vs RANIBIZUMAB