Cymbalta Side Effects
How can Cymbalta Side Effects affect You? | PatientsVille.com
View and Submit Cymbalta Side Effects
Your Cymbalta Side Effect submission can play a very important role. Reporting your experience could help identify an unknown risk and inform other patients and health care professionals.
Record and Track Your Side Effects
It is very important to keep track of all side effects and discuss them with your doctor. If you think you may have a medical emergency, call your doctor or 911 immediately.
Most drugs have a large list of nonsevere or mild adverse effects which do not rule out continued usage. These effects depend on individual sensitivity, and can include nausea, dizziness, diarrhea, malaise, vomiting, headache, dermatitis, dry mouth, etc. Check commonly reported side effects . These can be considered a form of pseudo-allergic reaction, as not all users experience these effects; many users experience none at all.
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
Alternative CYMBALTA Names:DULOXETIN
Active Ingredient: DULOXETIN
Side Effects reported to FDA: 12903. View Cymbalta Adverse Reports
Cymbalta safety alerts: 2005
Reported deaths: 747
Reported hospitalizations: 3368
Cymbalta (duloxetine) Public Health Advisory: Suicidality in Adults Being Treated with Antidepressant Medications
Audience: Neuropsychiatric healthcare professionals and consumers
[UPDATE 07/08/2005] FDA notified healthcare professionals about the availability of updated Healthcare Professional and Patient Information Sheets for antidepressant medications that were the subject of a June 30, 2005 Public Health Advisory issued about the risk of suicidality (suicidal thinking or behavior) in adults being treated with antidepressant medications.
[Posted 07/01/2005] In response to recent scientific publications that report the possibility of increased risk of suicidal behavior in adults treated with antidepressants, the FDA has issued a Public Health Advisory to update patients and healthcare providers with the latest information on this subject. Even before the publication of these recent reports, FDA had already begun the process of reviewing available data to determine whether there is an increased risk of suicidal behavior in adults taking antidepressants. The Agency has asked manufacturers to provide information from their trials using an approach similar to that used in the evaluation of the risk of suicidal behavior in the pediatric population taking antidepressants. This effort will involve hundreds of clinical trials and may take more than a year to complete.
[July 08, 2005 - Healthcare Professional and Patient Information Sheets - FDA]
Cymbalta Adverse Reactions
Nausea ( 1197 Reports)|Dizziness ( 1116 Reports)|Headache ( 807 Reports)|Feeling Abnormal ( 777 Reports)|Fatigue ( 673 Reports)|Depression ( 667 Reports)|Insomnia ( 648 Reports)|Alanine Aminotransferase Increased ( 586 Reports)|Anxiety ( 554 Reports)|Aspartate Aminotransferase Increased ( 509 Reports)|Diarrhoea ( 486 Reports)|Paraesthesia ( 482 Reports)|Hyperhidrosis ( 459 Reports)|Blood Pressure Increased ( 440 Reports)|Hepatic Enzyme Increased ( 430 Reports)|Suicidal Ideation ( 428 Reports)|Loss Of Consciousness ( 375 Reports)|Asthenia ( 374 Reports)|Vomiting ( 372 Reports)|Somnolence ( 366 Reports)|Fall ( 365 Reports)|Pain ( 362 Reports)|Confusional State ( 356 Reports)|Malaise ( 356 Reports)|Tremor ( 339 Reports)|Crying ( 334 Reports)|Agitation ( 301 Reports)|Dyspnoea ( 288 Reports)|Hypertension ( 278 Reports)|Convulsion ( 267 Reports)|