Does OCTREOTIDE Cause Product administration error? 81 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 81 reports of Product administration error have been filed in association with OCTREOTIDE (Octreotide Acetate). This represents 0.3% of all adverse event reports for OCTREOTIDE.
81
Reports of Product administration error with OCTREOTIDE
0.3%
of all OCTREOTIDE reports
4
Deaths
21
Hospitalizations
How Dangerous Is Product administration error From OCTREOTIDE?
Of the 81 reports, 4 (4.9%) resulted in death, 21 (25.9%) required hospitalization, and 3 (3.7%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OCTREOTIDE. However, 81 reports have been filed with the FAERS database.
What Other Side Effects Does OCTREOTIDE Cause?
Death (3,801)
Diarrhoea (3,621)
Fatigue (2,933)
Blood pressure increased (2,799)
Needle issue (2,740)
Malaise (2,737)
Pain (2,366)
Blood pressure systolic increased (2,340)
Malignant neoplasm progression (2,306)
Nausea (2,294)
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 OCTREOTIDE Alternatives Have Lower Product administration error Risk?
OCTREOTIDE vs OCTREOTIDE\OCTREOTIDE
OCTREOTIDE vs ODEVIXIBAT
OCTREOTIDE vs OFATUMUMAB
OCTREOTIDE vs OFLOXACIN
OCTREOTIDE vs OLANZAPINE