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YAZ, Yasmin, Ocella and Zarah

A New Form of Birth Control with New Health Risks

YAZ, Yasmin, Ocella and Zarah are a new form of birth control that comes with unique and potentially deadly side effects.

Yasmin (and its generic forms Zarah and Ocella) and YAZ are a similar type of birth control, but they have slightly different levels of one of their active ingredients.  Yasmin is the older of the two.  Yasmin was initially manufactured by Berlex Laboratories, a U.S. division of German pharmaceutical giant Schering AG.  Berlex obtained approval for the sale of Yasmin in the United States from the Food and Drug Administration (FDA) in April 2001.  Bayer acquired Berlex in 2006.  Then, in order to keep their market share, Bayer introduced YAZ, which slightly altered the formula of Yasmin.

YAZ and Yasmin differ in their dosing schedule and the amount of ethinyl estradiol (estrogen) they contain. Yasmin birth control uses a 21/7 dosing schedule.  This means that for 21 days, women take the regular Yasmin pills, which are yellow.  For the last 7 days of their cycle, they take the white pills, which have no active ingredients.  YAZ birth control has a 24/4 dosing schedule.  For the first 24 days, women take the pink tablets, which contain the active ingredients.  For the last 4 days, they take the white tablets, which contain no active ingredients.  The differing dosing schedule reflects the fact that Yasmin has 30 mcg. of ethinyl estradiol, while YAZ has only 20 mcg.

Despite the above differences, YAZ and Yasmin both contain the same dosage of drospirenone (drsp), which is the ingredient that makes YAZ/Yasmin birth control particularly dangerous.  Zarah and Ocella are the generic equivalents of Yasmin, so they, too, contain drospirenone.

The YAZ lawyers and YAZ attorneys at DeCarli Law are evaluating and investigating YAZ side effect lawsuits and Yasmin side effect lawsuits.  Contact DeCarli Law for a free consultation if you or a loved one may have experienced a side effect of YAZ, Yasmin, Ocella or Zarah.

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Address: 50 California Street, Suite 1500 San Francisco CA 94111 Toll Free: 1-800-401-4720 Phone: 1-415-738-6144
Debra DeCarli and Bob DeCarli are licensed by the State Bar of Texas and the State Bar of California.

DeCarli Law represents drug side effects and defective medical devices personal injury clients for claims, lawsuits and settlements in Alabama AL, Alaska AK, Arizona AZ, Arkansas AR, California CA, Colorado CO, Connecticut CT, Delaware DE, Georgia GA, Hawaii HI, Idaho ID, Illinois IL, Kansas KS, Maine ME, Maryland MD, Massachusetts MS, Minnesota MN, Mississippi MS, Montana MT, Nebraska NE, New Hampshire NH, New Jersey NJ, New Mexico NM, New York NY, North Carolina NC, North Dakota ND, Oklahoma OK, Oregon OR, Rhode Island RI, South Carolina SC, South Dakota SD, Tennessee TN, Utah UT, Vermont VT, Virginia VA, Washington WA, Washington D.C, West Virginia WV, Wisconsin WI and Wyoming WY. The attorneys of DeCarli Law are licensed in California and Texas. DeCarli Law's practice includes lawsuits for Propecia side effects, Finasteride lawsuits, Topamax lawsuits, Fosamax lawsuits, Gadolinium lawsuits, NSF lawsuits, Nephrogenic Systemic Fibrosis Lawsuits, YAZ lawsuits, Yasmin lawsuits, Ocella lawsuits, and Zarah lawsuits.