Does RITODRINE Cause Product use in unapproved indication? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Product use in unapproved indication have been filed in association with RITODRINE. This represents 4.3% of all adverse event reports for RITODRINE.
11
Reports of Product use in unapproved indication with RITODRINE
4.3%
of all RITODRINE reports
1
Deaths
7
Hospitalizations
How Dangerous Is Product use in unapproved indication From RITODRINE?
Of the 11 reports, 1 (9.1%) resulted in death, 7 (63.6%) required hospitalization, and 3 (27.3%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RITODRINE. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does RITODRINE Cause?
Exposure during pregnancy (82)
Foetal exposure during pregnancy (79)
Premature baby (71)
Maternal exposure during pregnancy (67)
Low birth weight baby (51)
Premature delivery (38)
Pulmonary oedema (30)
Anaemia (14)
Respiratory failure (13)
Emotional disorder (12)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which RITODRINE Alternatives Have Lower Product use in unapproved indication Risk?
RITODRINE vs RITONAVIR
RITODRINE vs RITUXAN
RITODRINE vs RITUXIMAB
RITODRINE vs RITUXIMAB-ABBS
RITODRINE vs RITUXIMAB-ARRX