Does ABALOPARATIDE Cause Product dose omission? 938 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 938 reports of Product dose omission have been filed in association with ABALOPARATIDE (Tymlos). This represents 4.0% of all adverse event reports for ABALOPARATIDE.
938
Reports of Product dose omission with ABALOPARATIDE
4.0%
of all ABALOPARATIDE reports
1
Deaths
64
Hospitalizations
How Dangerous Is Product dose omission From ABALOPARATIDE?
Of the 938 reports, 1 (0.1%) resulted in death, 64 (6.8%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABALOPARATIDE. However, 938 reports have been filed with the FAERS database.
What Other Side Effects Does ABALOPARATIDE Cause?
Headache (4,048)
Nausea (3,134)
Dizziness (3,005)
Fatigue (2,637)
Heart rate increased (2,092)
Palpitations (1,730)
Arthralgia (1,711)
Bone pain (1,360)
Back pain (1,229)
Pain (1,191)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which ABALOPARATIDE Alternatives Have Lower Product dose omission Risk?
ABALOPARATIDE vs ABATACEPT
ABALOPARATIDE vs ABATACEPT SUBQ /ML
ABALOPARATIDE vs ABCIXIMAB
ABALOPARATIDE vs ABEMACICLIB
ABALOPARATIDE vs ABILIFY