Does THIOTEPA Cause Respiratory distress? 53 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 53 reports of Respiratory distress have been filed in association with THIOTEPA (Thiotepa). This represents 0.8% of all adverse event reports for THIOTEPA.
53
Reports of Respiratory distress with THIOTEPA
0.8%
of all THIOTEPA reports
20
Deaths
32
Hospitalizations
How Dangerous Is Respiratory distress From THIOTEPA?
Of the 53 reports, 20 (37.7%) resulted in death, 32 (60.4%) required hospitalization, and 9 (17.0%) were considered life-threatening.
Is Respiratory distress Listed in the Official Label?
Yes, Respiratory distress is listed as a known adverse reaction in the official FDA drug label for THIOTEPA.
What Other Side Effects Does THIOTEPA Cause?
Off label use (762)
Febrile neutropenia (645)
Mucosal inflammation (616)
Cytomegalovirus infection (446)
Product use in unapproved indication (425)
Pyrexia (359)
Drug ineffective (358)
Acute graft versus host disease in skin (355)
Acute graft versus host disease (331)
Cytomegalovirus infection reactivation (325)
What Other Drugs Cause Respiratory distress?
PREDNISONE (519)
CYCLOPHOSPHAMIDE (496)
METHOTREXATE (445)
DEXAMETHASONE (431)
RITUXIMAB (420)
TACROLIMUS (376)
ALBUTEROL (355)
TREPROSTINIL (345)
VINCRISTINE (342)
PREDNISOLONE (298)
Which THIOTEPA Alternatives Have Lower Respiratory distress Risk?
THIOTEPA vs THIOTHIXENE
THIOTEPA vs THROMBIN
THIOTEPA vs THROMBIN HUMAN
THIOTEPA vs THYMOCYTE IMMUNE GLOBULIN NOS
THIOTEPA vs THYMOGLOBULINE