Does ABALOPARATIDE Cause Intentional dose omission? 623 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 623 reports of Intentional dose omission have been filed in association with ABALOPARATIDE (Tymlos). This represents 2.7% of all adverse event reports for ABALOPARATIDE.
623
Reports of Intentional dose omission with ABALOPARATIDE
2.7%
of all ABALOPARATIDE reports
1
Deaths
104
Hospitalizations
How Dangerous Is Intentional dose omission From ABALOPARATIDE?
Of the 623 reports, 1 (0.2%) resulted in death, 104 (16.7%) required hospitalization, and 1 (0.2%) were considered life-threatening.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABALOPARATIDE. However, 623 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 Intentional dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
SOFOSBUVIR\VELPATASVIR (474)
Which ABALOPARATIDE Alternatives Have Lower Intentional dose omission Risk?
ABALOPARATIDE vs ABATACEPT
ABALOPARATIDE vs ABATACEPT SUBQ /ML
ABALOPARATIDE vs ABCIXIMAB
ABALOPARATIDE vs ABEMACICLIB
ABALOPARATIDE vs ABILIFY