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Sinequan Related Fatigue

Official Government Database Reports35
Online Conversations4

Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients. To view the active ingredient report, please click here.

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Druginformer Identified Side Effects: Fatigue, Nightmare, Depression, Dry mouth, Weight increased

Posted By Anonymous in askapatient.com on January 31, 2015 @ 12:00 am

Side Effects: exhaustion, weight gain, depression, dry mouth and the rest of my body, nightmares unless I added a seroquel I am reducing 10 milligrams every 2 weeks, and it's a nightmare. a...

Druginformer Identified Side Effects: Fatigue, Dry mouth

Posted By Anonymous in askapatient.com on January 3, 2014 @ 12:00 am

Side Effects: Dry mouth, tired next day.

Druginformer Identified Side Effects: Fatigue, Hunger, Abnormal weight gain, Sedation, Increased appetite, Scar, Somnolence

Posted By Anonymous in askapatient.com on January 7, 2013 @ 12:00 am

Side Effects: I had to come off seroquel because it was making me so tired all day. This drug makes me tired at night, but doesn't knock me out like seroquel. It also doesn't make me tired all day li...

Druginformer Identified Side Effects: Fatigue

Posted By Anonymous in askapatient.com on January 4, 2011 @ 12:00 am

Side Effects: initially very tired. This medicine has been the ONLY thing that has helped my miserable skin. OK prednisone too but you can't take it long term. I am currently trying a very...

* Warning: The facts and figures contained in these reports are accurate to the best of our capability; however, our metrics are only meant to augment your medical knowledge, and should never be used as the sole basis for selecting a new medication. As with any medical decision, be sure to work with your doctor to ensure the best choices are made for your condition.

* About FAERS: The FDA Adverse Event Reporting System (FAERS) is used by FDA for activities such as looking for new safety concerns that might be related to a marketed product, evaluating a manufacturer's compliance to reporting regulations and responding to outside requests for information. Reporting of adverse events is a voluntary process, and not every report is sent to FDA and entered into FAERS. The FAERS database may contain duplicate reports, the report quality is variable, and many factors may influence reporting (e.g., media attention, length of time a drug is marketed, market share). For these reasons, FAERS case reports cannot be used to calculate incidence or estimates of risk for a particular product or compare risks between products.