Does ABALOPARATIDE Cause Wrong technique in product usage process? 689 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 689 reports of Wrong technique in product usage process have been filed in association with ABALOPARATIDE (Tymlos). This represents 3.0% of all adverse event reports for ABALOPARATIDE.
689
Reports of Wrong technique in product usage process with ABALOPARATIDE
3.0%
of all ABALOPARATIDE reports
1
Deaths
15
Hospitalizations
How Dangerous Is Wrong technique in product usage process From ABALOPARATIDE?
Of the 689 reports, 1 (0.1%) resulted in death, 15 (2.2%) required hospitalization.
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 ABALOPARATIDE. However, 689 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 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 ABALOPARATIDE Alternatives Have Lower Wrong technique in product usage process Risk?
ABALOPARATIDE vs ABATACEPT
ABALOPARATIDE vs ABATACEPT SUBQ /ML
ABALOPARATIDE vs ABCIXIMAB
ABALOPARATIDE vs ABEMACICLIB
ABALOPARATIDE vs ABILIFY