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Brevicon 28-day

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* Based on 4 reviews from across the web.
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  Please use Workbench for in-depth research on Brevicon 28-day.

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

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Druginformer Identified Side Effects: Nausea, Abdominal distension, Depression, Decreased appetite

Posted By Anonymous in askapatient.com on May 20, 2013 @ 12:00 am

Side Effects: Nausea, decrease in appetite, feeling bloated, even slight depression.

Druginformer Identified Side Effects: Swelling, Tenderness, Vision blurred, Weight increased, Menstruation irregular

Posted By Anonymous in askapatient.com on June 27, 2008 @ 12:00 am

Side Effects: Swelling of breasts and tenderness, weight gain, blurry vision, spotting in the third week Have only been on it for two months and just started third month. Vision problems a...

Druginformer Identified Side Effects: Nausea, Weight increased

Posted By Anonymous in askapatient.com on October 19, 2006 @ 12:00 am

Side Effects: Intially had nausea from it. Had to take the pill at night so as to sleep through the nausea. Weight gain. Had severe periods, anemia and PMS. My family (and I) were happy ...

Druginformer Identified Side Effects: Breast tenderness, Abdominal discomfort, Abdominal distension, Libido decreased, Weight increased

Posted By Anonymous in askapatient.com on August 26, 2005 @ 12:00 am

Side Effects: severe breast tenderness that lasted ALL month, complete loss of libido due to this, felt sick to my stomach al the time too, bloating and weight gain of about 5 pounds switch...


* 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.