Does SAPROPTERIN Cause Product dose omission? 63 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 63 reports of Product dose omission have been filed in association with SAPROPTERIN (JAVYGTOR). This represents 1.1% of all adverse event reports for SAPROPTERIN.
63
Reports of Product dose omission with SAPROPTERIN
1.1%
of all SAPROPTERIN reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product dose omission From SAPROPTERIN?
Of the 63 reports, 3 (4.8%) 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 SAPROPTERIN. However, 63 reports have been filed with the FAERS database.
What Other Side Effects Does SAPROPTERIN Cause?
Drug ineffective (356)
Therapy non-responder (348)
Headache (309)
Maternal exposure during pregnancy (277)
Vomiting (260)
Diarrhoea (238)
Amino acid level increased (194)
Nausea (189)
Abdominal pain upper (179)
Anxiety (174)
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 SAPROPTERIN Alternatives Have Lower Product dose omission Risk?
SAPROPTERIN vs SAQUINAVIR
SAPROPTERIN vs SARECYCLINE
SAPROPTERIN vs SARGRAMOSTIM
SAPROPTERIN vs SARILUMAB
SAPROPTERIN vs SATRALIZUMAB