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Cenestin Related Night sweats

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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: Night sweats, Mood swings, Hot flush

Posted By jmklh in fdb.rxlist.com on March 29, 2010 @ 12:00 am

I have been taking Cenestin for several years and I have felt like a new person ever since. Mood swings, hot flashes and night sweats are gone. Intimacy has become improved considerably.

Druginformer Identified Side Effects: Night sweats, Hot flush

Posted By Anonymous in askapatient.com on January 30, 2010 @ 12:00 am

Side Effects: hot flashes, night sweats due to ovary removed. I take cenestin with prometrium. I've had no side effects. People tell me I look 25 years younger than I am.

Druginformer Identified Side Effects: Night sweats, Hysterectomy, Ovarian cancer, Endometrial cancer, Weight increased

Posted By Anonymous in askapatient.com on January 18, 2010 @ 12:00 am

Side Effects: started cenestin after the hysterectomy in 2001. Kept asking the Dr. if it was safe. I had read that you should only take it short term. Still had night sweats and weight gain from it. ...

Druginformer Identified Side Effects: Night sweats

Posted By Anonymous in askapatient.com on February 4, 2009 @ 12:00 am

Side Effects: none Second night after surgery I had a night sweat. My Dr. had me on 0.9 censetin the day I left the hospital. I do not have no night sweats at all. I am just scared a little...


* 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.