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Cenestin

Average User Review Score
* Based on 69 reviews from across the web.
Wikipedia

Conjugated estrogens, or conjugated equine estrogens (CEEs), are blended equine estrogens, which may include estrone sulfate, equilin sulfate, and equilenin sulfate. CEEs are used clinically in hormone replacement therapy, with marketed products including both natural preparations isolated from the urine of pregnant mares (brand names Premarin) as well as fully synthetic replications of the natural preparations (brand names Cenestin, Enjuvia, Congest, and C.E.S.). Prempro and Premphase are combination formulations of natural CEEs with medroxyprogesterone acetate.

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* Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients.

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Druginformer Identified Side Effects: None

Posted By Heartscanner in fdb.rxlist.com on July 13, 2015 @ 12:00 am

I had total hysterectomy in 2004. Patches didn't work. Cenestin was the best. No hot flashes, night sweats, felt wonderful. Now the Company isn't making it any more. I have tried Several others and ...

Druginformer Identified Side Effects: Weight increased

Posted By Mad as Heck in fdb.rxlist.com on April 5, 2015 @ 12:00 am

After a complete hysterectomy putting me into surgical menopause, I tried so many different medications, patches included, I can't remember what they were. At one point I gained 25 lbs. in a month. M...

Druginformer Identified Side Effects: None

Posted By LIZ in fdb.rxlist.com on January 22, 2015 @ 12:00 am

I HAD BEEN TAKING CENESTIN FOR 13 YEARS WITH GREAT RESULTS. THEN I COULD NOT GET IT ANYMORE AND I WAS PUT ON PREMARIN. AFTER ONLY A FEW WEEKS MY HAIR WAS FALLING OUT, BRITTLE NAILS, 7/24 HEARTBURN SO ...

Druginformer Identified Side Effects: None

Posted By Anonymous in askapatient.com on December 1, 2014 @ 12:00 am

Side Effects: None I've taken Cenestin for 10yrs due to hysterectomy. I was dx with aggressive breast cancer in 2012, but it was NOT fed by estrogen or progesterone. It was Her2+. I stopped...

Druginformer Identified Side Effects: None

Posted By Anonymous in fdb.rxlist.com on September 3, 2014 @ 12:00 am

I've used Cenestin .625 since 1999 and have loved it. I've felt great! I just found out today that the manufacturer Teva is no longer making it. I'm not sure what I'm going to do now. I hope there...

Druginformer Identified Side Effects: None

Posted By afinch in fdb.rxlist.com on August 23, 2014 @ 12:00 am

I have been taken this medication for 14 years and it is very good. I do not have and of the bad thing that goes along with the change of life thank God. Then I was changed to Premarin 1.25 and this w...

Druginformer Identified Side Effects: Hysterectomy, Endometrial cancer

Posted By Debby in fdb.rxlist.com on August 10, 2014 @ 12:00 am

Had a complete hysterectomy in 2001. Dr. prescribed cenestin and I was on it for 7 years. Maybe it worked for hot flashes, etc. however, I wish I would have never heard of this drug because in 2008, w...

Druginformer Identified Side Effects: None

Posted By Anonymous in askapatient.com on July 18, 2014 @ 12:00 am

Side Effects: This is the only HRT that works for me. There have been times that it has not been available and I got a generic and my symptoms returned.

Druginformer Identified Side Effects: None

Posted By FabuCat in fdb.rxlist.com on June 4, 2014 @ 12:00 am

Reports of Cenestin being discontinued are inaccurate. First I checked with the FDA and it is not on the discontinued list (6 months warning required). The FDA gave me the manufacturer's phone number...

Druginformer Identified Side Effects: None

Posted By Anonymous in fdb.rxlist.com on March 21, 2014 @ 12:00 am

Cenestin Has worked great for me for many years and now they have quit making it so I have to switch to another, not happy!!!!


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* 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.