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increased thirst joint or muscle pain large, hive-like swelling on the face, eyelids, lips, tongue, throat, hands, legs, feet, or sex organs light-colored stools loss of
Nausea, dry mouth, constipation, loss of appetite, tiredness, drowsiness, or increased sweating may occur
Common side effects of Cymbalta include nausea, dry mouth, constipation, diarrhea, fatigue, difficulty sleeping, and dizziness, and sexual dysfunction ( decreased sex drive
Duloxetine therapy can be associated with transient asymptomatic elevations in serum aminotransferase levels and has been linked to rare instances of clinically apparent acute liver injury
Negative experiences at home, at school, or in the community have a damaging effect on the
It is created by eHealthMe based on reports of 3,648 people who have interactions when taking Cymbalta and Norco from the FDA, and is updated regularly
Nausea, dry mouth, constipation, loss of appetite, tiredness, drowsiness, or increased sweating may occur
Here are some examples of side effects commonly reported with Cymbalta treatment:
dizziness
In clinical studies, both weight gain and weight loss were reported in adults who took Cymbalta, but these weight changes weren’t common
Antenatal use of antidepressants and risks of teratogenicity and adverse pregnancy outcomes: Drugs other than selective serotonin reuptake inhibitors; Atypical antidepressants: Pharmacology, administration, and side effects; Clinical manifestations and diagnosis of stress (takotsubo) cardiomyopathy; Discontinuing antidepressant
A 2021 review of Cymbalta clinical trials found that participants who took the drug were more likely to experience common side effects than those who took a placebo
Adverse Event - An event in which care resulted in an undesirable clinical outcome-an outcome not caused by
Other bleeding events related to SSRI and SNRI use have ranged from ecchymoses, hematomas, epistaxis, and petechiae to life-threatening hemorrhages
[1] An AE is a harmful and negative outcome that happens when a patient has been provided with medical care
These common side effects of duloxetine can happen in up to 1 in 10 people
Safety data from all placebo-controlled trials of duloxetine conducted between December 1993 and December 2010, and post-marketing reports from duloxetine-treated patients in the US Food and Drug Administration Adverse Event Reporting System (FAERS), were searched for bleeding-related treatment-emergent