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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does GLASDEGIB Cause Hypoxia? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Hypoxia have been filed in association with GLASDEGIB (Daurismo). This represents 1.0% of all adverse event reports for GLASDEGIB.

5
Reports of Hypoxia with GLASDEGIB
1.0%
of all GLASDEGIB reports
0
Deaths
4
Hospitalizations

How Dangerous Is Hypoxia From GLASDEGIB?

Of the 5 reports, 4 (80.0%) required hospitalization, and 2 (40.0%) were considered life-threatening.

Is Hypoxia Listed in the Official Label?

Yes, Hypoxia is listed as a known adverse reaction in the official FDA drug label for GLASDEGIB.

What Other Side Effects Does GLASDEGIB Cause?

Death (102) Febrile neutropenia (86) Pneumonia (50) Off label use (29) Neoplasm progression (28) Neutropenia (26) Electrocardiogram qt prolonged (18) Sepsis (18) Pyrexia (17) Septic shock (16)

What Other Drugs Cause Hypoxia?

TREPROSTINIL (1,322) PREDNISONE (898) MACITENTAN (845) ALBUTEROL (763) CYCLOPHOSPHAMIDE (749) PACLITAXEL (684) DEXAMETHASONE (628) AMBRISENTAN (613) TIOTROPIUM (582) ACETAMINOPHEN (545)

Which GLASDEGIB Alternatives Have Lower Hypoxia Risk?

GLASDEGIB vs GLATIRAMER GLASDEGIB vs GLECAPREVIR\PIBRENTASVIR GLASDEGIB vs GLEEVEC GLASDEGIB vs GLICLAZIDE GLASDEGIB vs GLIMEPIRIDE

Related Pages

GLASDEGIB Full Profile All Hypoxia Reports All Drugs Causing Hypoxia GLASDEGIB Demographics