Does LANREOTIDE Cause Incorrect product administration duration? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Incorrect product administration duration have been filed in association with LANREOTIDE (Lanreotide Acetate). This represents 0.2% of all adverse event reports for LANREOTIDE.
17
Reports of Incorrect product administration duration with LANREOTIDE
0.2%
of all LANREOTIDE reports
1
Deaths
5
Hospitalizations
How Dangerous Is Incorrect product administration duration From LANREOTIDE?
Of the 17 reports, 1 (5.9%) resulted in death, 5 (29.4%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LANREOTIDE. However, 17 reports have been filed with the FAERS database.
What Other Side Effects Does LANREOTIDE Cause?
Diarrhoea (1,646)
Off label use (1,536)
Death (1,177)
Fatigue (1,022)
Nausea (775)
Abdominal pain (662)
Injection site pain (618)
Malaise (520)
Headache (515)
Asthenia (483)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which LANREOTIDE Alternatives Have Lower Incorrect product administration duration Risk?
LANREOTIDE vs LANSOPRAZOLE
LANREOTIDE vs LANTHANUM
LANREOTIDE vs LANTUS
LANREOTIDE vs LANTUS SOLOSTAR
LANREOTIDE vs LAPATINIB