Does LENOGRASTIM Cause Product administration error? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product administration error have been filed in association with LENOGRASTIM (GUNA-GCSF). This represents 0.7% of all adverse event reports for LENOGRASTIM.
5
Reports of Product administration error with LENOGRASTIM
0.7%
of all LENOGRASTIM reports
5
Deaths
5
Hospitalizations
How Dangerous Is Product administration error From LENOGRASTIM?
Of the 5 reports, 5 (100.0%) resulted in death, 5 (100.0%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LENOGRASTIM. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does LENOGRASTIM Cause?
Pyrexia (95)
Vomiting (61)
Neutropenia (59)
Dyspnoea (55)
Fatigue (55)
Nausea (53)
Pneumonia (51)
Arthralgia (50)
Febrile neutropenia (50)
Off label use (50)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which LENOGRASTIM Alternatives Have Lower Product administration error Risk?
LENOGRASTIM vs LENVATINIB
LENOGRASTIM vs LEPONEX
LENOGRASTIM vs LERCANIDIPINE
LENOGRASTIM vs LETAIRIS
LENOGRASTIM vs LETERMOVIR