Does ABALOPARATIDE Cause Product quality issue? 914 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 914 reports of Product quality issue have been filed in association with ABALOPARATIDE (Tymlos). This represents 3.9% of all adverse event reports for ABALOPARATIDE.
914
Reports of Product quality issue with ABALOPARATIDE
3.9%
of all ABALOPARATIDE reports
1
Deaths
26
Hospitalizations
How Dangerous Is Product quality issue From ABALOPARATIDE?
Of the 914 reports, 1 (0.1%) resulted in death, 26 (2.8%) required hospitalization.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABALOPARATIDE. However, 914 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which ABALOPARATIDE Alternatives Have Lower Product quality issue Risk?
ABALOPARATIDE vs ABATACEPT
ABALOPARATIDE vs ABATACEPT SUBQ /ML
ABALOPARATIDE vs ABCIXIMAB
ABALOPARATIDE vs ABEMACICLIB
ABALOPARATIDE vs ABILIFY