Does HYDROXYPROGESTERONE CAPROATE Cause Product administration error? 972 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 972 reports of Product administration error have been filed in association with HYDROXYPROGESTERONE CAPROATE (Hydroxyprogesterone Caproate). This represents 4.3% of all adverse event reports for HYDROXYPROGESTERONE CAPROATE.
972
Reports of Product administration error with HYDROXYPROGESTERONE CAPROATE
4.3%
of all HYDROXYPROGESTERONE CAPROATE reports
0
Deaths
64
Hospitalizations
How Dangerous Is Product administration error From HYDROXYPROGESTERONE CAPROATE?
Of the 972 reports, 64 (6.6%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HYDROXYPROGESTERONE CAPROATE. However, 972 reports have been filed with the FAERS database.
What Other Side Effects Does HYDROXYPROGESTERONE CAPROATE Cause?
Premature delivery (4,322)
Premature baby (3,930)
Injection site pain (2,572)
Injection site pruritus (1,841)
Product dose omission issue (1,663)
Inappropriate schedule of product administration (1,164)
Injection site swelling (924)
Injection site mass (829)
Injection site erythema (743)
Preterm premature rupture of membranes (694)
What Other Drugs Cause Product administration error?
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
HYDROCHLOROTHIAZIDE\OLMESARTAN MEDOXOMIL (222)
Which HYDROXYPROGESTERONE CAPROATE Alternatives Have Lower Product administration error Risk?
HYDROXYPROGESTERONE CAPROATE vs HYDROXYPROPYL CELLULOSE
HYDROXYPROGESTERONE CAPROATE vs HYDROXYUREA
HYDROXYPROGESTERONE CAPROATE vs HYDROXYZINE
HYDROXYPROGESTERONE CAPROATE vs HYDROXYZINE\HYDROXYZINE
HYDROXYPROGESTERONE CAPROATE vs HYOSCYAMINE