Does OCTREOTIDE Cause Wrong technique in product usage process? 344 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 344 reports of Wrong technique in product usage process have been filed in association with OCTREOTIDE (Octreotide Acetate). This represents 1.5% of all adverse event reports for OCTREOTIDE.
344
Reports of Wrong technique in product usage process with OCTREOTIDE
1.5%
of all OCTREOTIDE reports
24
Deaths
119
Hospitalizations
How Dangerous Is Wrong technique in product usage process From OCTREOTIDE?
Of the 344 reports, 24 (7.0%) resulted in death, 119 (34.6%) required hospitalization, and 14 (4.1%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OCTREOTIDE. However, 344 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which OCTREOTIDE Alternatives Have Lower Wrong technique in product usage process Risk?
OCTREOTIDE vs OCTREOTIDE\OCTREOTIDE
OCTREOTIDE vs ODEVIXIBAT
OCTREOTIDE vs OFATUMUMAB
OCTREOTIDE vs OFLOXACIN
OCTREOTIDE vs OLANZAPINE