Does DULOXETINE Cause Exposure during breast feeding? 59 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 59 reports of Exposure during breast feeding have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.1% of all adverse event reports for DULOXETINE.
59
Reports of Exposure during breast feeding with DULOXETINE
0.1%
of all DULOXETINE reports
1
Deaths
9
Hospitalizations
How Dangerous Is Exposure during breast feeding From DULOXETINE?
Of the 59 reports, 1 (1.7%) resulted in death, 9 (15.3%) required hospitalization, and 1 (1.7%) were considered life-threatening.
Is Exposure during breast feeding Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 59 reports have been filed with the FAERS database.
What Other Side Effects Does DULOXETINE Cause?
Nausea (7,355)
Dizziness (6,983)
Drug withdrawal syndrome (6,503)
Headache (5,541)
Fatigue (5,309)
Insomnia (5,270)
Anxiety (4,973)
Paraesthesia (4,854)
Drug ineffective (4,829)
Hyperhidrosis (4,101)
What Other Drugs Cause Exposure during breast feeding?
COPPER (412)
ADALIMUMAB (215)
FLUOXETINE (122)
NEVIRAPINE (117)
BUPRENORPHINE (110)
LAMIVUDINE (102)
LEVONORGESTREL (102)
ZIDOVUDINE (93)
BUPRENORPHINE\NALOXONE (83)
NICOTINE (81)
Which DULOXETINE Alternatives Have Lower Exposure during breast feeding Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB