Does ESTRADIOL\LEVONORGESTREL Cause Wrong technique in product usage process? 246 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 246 reports of Wrong technique in product usage process have been filed in association with ESTRADIOL\LEVONORGESTREL. This represents 19.6% of all adverse event reports for ESTRADIOL\LEVONORGESTREL.
246
Reports of Wrong technique in product usage process with ESTRADIOL\LEVONORGESTREL
19.6%
of all ESTRADIOL\LEVONORGESTREL reports
0
Deaths
0
Hospitalizations
How Dangerous Is Wrong technique in product usage process From ESTRADIOL\LEVONORGESTREL?
Of the 246 reports.
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 ESTRADIOL\LEVONORGESTREL. However, 246 reports have been filed with the FAERS database.
What Other Side Effects Does ESTRADIOL\LEVONORGESTREL Cause?
Product adhesion issue (554)
Product physical issue (305)
Device adhesion issue (195)
Hot flush (127)
Drug ineffective (126)
Application site rash (90)
Device breakage (87)
Drug dose omission (81)
Product quality issue (81)
Application site pruritus (63)
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 ESTRADIOL\LEVONORGESTREL Alternatives Have Lower Wrong technique in product usage process Risk?
ESTRADIOL\LEVONORGESTREL vs ESTRADIOL\NORETHINDRONE
ESTRADIOL\LEVONORGESTREL vs ESTRADIOL\NORETHINDRONE\RELUGOLIX
ESTRADIOL\LEVONORGESTREL vs ESTRADIOL\PROGESTERONE
ESTRADIOL\LEVONORGESTREL vs ESTRAMUSTINE
ESTRADIOL\LEVONORGESTREL vs ESTRING