Did you or a loved one take Yaz, Yasmin or Ocella birth control? Did you or a loved one suffer a blood clot, stroke or gallbladder disease? We can help.
Law Offices of Sadaka Associates is filing lawsuits on behalf of women who suffered heart attacks, cardiac arrhythmias, blood clots, deep vein thrombosis (DVT), pulmonary embolism (PE), strokes, gallbladder disease, hepatic adenomas or benign liver tumors, and other serious injuries and sudden death.
What is Yaz, Yasmin and Ocella?
Yaz and Yasmin are the trade names for birth control pills manufactured by Bayer Healthcare Pharmaceuticals, Inc. Like most birth control pills, they contain a mixture of estrogen and progestin. Unlike most birth control pills, however, Yaz and Yasmin use a different type of progestin in combination with low dose estrogen.
Ocella is the generic form of Yaz and Yasmin and is manufactured by various generic drug manufacturers.
What is the problem with Yaz, Yasmin and Ocella?
The controversy surrounding Yaz, Yasmin and Ocella focuses on two points. The first is the products’ use a unique type of progestin that has been linked to excess elimination of urine leading to dehydration. The second is misleading direct-to-consumer advertising.
Birth Control Blood Clots
Birth control has long been associated with an increased risk of blood clots. Indeed, the risk of birth control related blood clots is in the warning label for all birth control drugs.
What is alleged to be different with Yaz, Yasmin and Ocella is the use a unique type of progestin that has been linked to excess elimination of urine leading to dehydration. Dehydration can cause an electrolyte imbalance in body leading to heart attack and arrhythmia. Dehydration can also increase the risk of the formation of blood clots.
Types of Birth Control Related Blood Clots
DVT Blood Clots
DVT or Deep Vein Thrombosis is a blood clot that is formed in the “deep veins” of the leg or arm. The blood clot blocks blood flow to the area and can cause a great deal of pain. In some instances, the DVT blood clots can dislodge and form blood clots in the lung (pulmonary embolism).
Blood Clots in the Lung
Blood clots in the lung or pulmonary embolism is a serious, life-threatening condition. What happens is that a blood clot forms in the the vein that leads from the heart to the lung blocking blood delivery. If the blockage is severe enough or untreated this can lead to death. The blood clot can start as a DVT blood clot ad travel to the lung or it can form directly in the lung.
Birth Control Related Stroke
Finally, birth control is related to an increased risk of stroke. Birth control related stroke can have long lasting effects on speech, hearing and cognitive function.
Misleading Advertising: Aren’t all Birth Control Pills Associated with a Risk of Blood Clots?
Yes. All birth control pills carry some risk of blood clots. However, on October 3, 2008, Bayer Healthcare Pharmaceuticals, Inc. received a warning letter from the FDA about misleading advertising (see reprint of the warning letter below). Why was the advertising misleading? Because Bayer downplayed the true risks of Yaz and Yasmin, making those pills appear safer than other brands when they carried the same if not greater risk of blood clots.
Contact Law Offices of Sadaka Associates for a Free Legal Consulation
If you or a loved one took the birth control Yaz, Yasmin or Ocella and suffered a blood clot then contact our lawyers today for a free legal consultation. Fill out our online form or call us at 1-800-810-3457.
FDA Warning Letter (10/3/2008)
Bayer HealthCare Pharmaceuticals, Inc. 03-Oct-08
Department of Health and Human Services
Public Health Service
Food and Drug Administration
Silver Spring, MD 20993
TRANSMITTED BY FACSIMILE
Reinhard Franzen
President & Chief Executive Officer
Bayer HealthCare Pharmaceuticals, Inc.
P.O. Box 1000
Montville, NJ 07045-1000
Re: NDA #21-676, 21-873, 22-045
YAZ® (drospirenone and ethinyl estradiol) Tablets
MACMIS ID# 16473
WARNING LETTER
Dear Mr. Franzen:
The Division of Drug Marketing, Advertising, and Communications (DDMAC) has reviewed two 60-second direct-to-consumer (DTC) broadcast television advertisements (TV Ads) entitled “Not Gonna Take it” (ZYRA-6323) and “Balloons” (ZYRA-6567) for YAZ® (drospirenone and ethinyl estradiol) Tablets (YAZ) submitted by Bayer HealthCare Pharmaceuticals, Inc. (Bayer) under cover of separate Forms FDA-2253. The TV Ads are misleading because they broaden the drug’s indication, overstate the efficacy of YAZ, and minimize serious risks associated with the use of the drug. Thus, the TV Ads misbrand the drug in violation of the Federal Food, Drug, and Cosmetic Act (the Act), 21 U.S.C. 352(n), 352(f)(1) & 321(n), and FDA’s implementing regulations. 21 CFR 201.100(c)(1); 201.128; 202.1(e)(5)(iii) & (e)(6)(i). These violations are concerning from a public health perspective because they encourage use of YAZ in circumstances other than those in which the drug has been approved, over-promise the benefits and minimize the risks associated with YAZ.
Background
According to the INDICATIONS AND USAGE section from the FDA-approved product labeling (PI), YAZ is approved for the following indications (in pertinent part):
[F]or the prevention of pregnancy in women who elect to use an oral contraceptive….
[F]or the treatment of symptoms of premenstrual dysphoric disorder (PMDD) in women who choose to use an oral contraceptive as their method of contraception. The effectiveness of YAZ for PMDD when used for more than three menstrual cycles has not been evaluated.
The essential features of PMDD according to the Diagnostic and Statistical Manual-4th edition (DSM-IV) include markedly depressed mood, anxiety or tension, affective lability, and persistent anger or irritability. Other features include decreased interest in usual activities, difficulty concentrating, lack of energy, change in appetite or sleep, and feeling out of control. Physical symptoms associated with PMDD include breast tenderness, headache, joint and muscle pain, bloating and weight gain. In this disorder, these symptoms occur regularly during the luteal phase and remit within a few days following onset of menses; the disturbance markedly interferes with work or school, or with usual social activities and relationships with others. Diagnosis is made by healthcare providers according to DSM-IV criteria, with symptomatology assessed prospectively over at least two menstrual cycles. In making the diagnosis, care should be taken to rule out other cyclical mood disorders.
YAZ has not been evaluated for the treatment of premenstrual syndrome (PMS) [emphasis added].
[F]or the treatment of moderate acne vulgaris in women at least 14 years of age, who have no known contraindications to oral contraceptive therapy and have achieved menarche. YAZ should be used for the treatment of acne only if the patient desires an oral contraceptive for birth control.
Additionally, the BRIEF SUMMARY PATIENT PACKAGE INSERT and DETAILED PATIENT PACKAGE INSERT state that:
… YAZ has not been shown to be effective for the treatment of premenstrual syndrome (PMS), a less serious cluster of symptoms occurring before menstruation. If you or your healthcare provider believes you have PMS, you should only take YAZ if you want to prevent pregnancy; and not for the treatment of PMS….
The PI for YAZ includes a BOXED WARNING that states (in pertinent part):
Cigarette smoking increases the risk of serious cardiovascular side effects from oral contraceptive use. This risk increases with age and with heavy smoking (15 or more cigarettes per day) and is quite marked in women over 35 years of age. Women who use oral contraceptives should be strongly advised not to smoke.
Additionally, there are numerous warnings associated with the use of YAZ including, but not limited to, venous and arterial thrombotic and thromboembolic events (such as myocardial infarction, thromboembolism, stroke), hepatic neoplasia, gallbladder disease, and hypertension.
Moreover, YAZ has additional risks because it contains the progestin, drospirenone. Drospirenone has antimineraloco rticoid properties which can lead to hyperkalemia in high risk patients, which may result in potentially serious heart and health problems. Women taking YAZ must be concerned about the drug interactions that could increase potassium, in addition to the drug interactions common to all combination oral contraceptives. This additional risk is described in the bolded WARNINGS section of YAZ’s PI.
Broadening of Indication
Premenstrual Dvsghoric Disorder (PMDD)
“Not Gonna Take It” (ZYRA-6323) & “Balloons” (ZYRA-6567)
The TV Ads misleadingly suggest that YAZ is effective in a broader range of patients and conditions than has been demonstrated by substantial evidence or substantial clinical experience. Specifically, given the overlap in certain symptoms between premenstrual syndrome (PMS) and PMDD, and the material limitation on YAZ’s PMDD indication (that it has not been evaluated for the treatment of the less serious condition, PMS), the TV Ads misleadingly suggest that YAZ is appropriate for treating women with PMS, who may not be appropriate candidates for this drug. We note that despite listing certain symptoms of PMDD, nowhere do the TV Ads use the full phrase “premenstrual dysphoric disorder,” to more completely distinguish PMDD from PMS, thereby increasing the likelihood that a viewer, in light of the claims and presentations described below, will understand it to be the same as, or substantially similar to, PMS.
The TV Ad ” Not Gonna Take It” starts by stating:
• “We all know that birth control pills are 99% effective and can give you shorter, lighter periods. But did you know there’s a Pill that could do more?”
It then displays images of energetic, euphoric, playful women singing “We’re Not Gonna Take It” as they kick, punch, and push words describing symptoms such as “IRRITABILITY,” “MOODINESS,” “BLOATING,” and “FEELING ANXIOUS,” away from the screen, followed by the claim “It’s YAZ! And there’s no other birth control like it.” The screen then displays a listing of symptoms including: irritability; increased appetite; moodiness; fatigue; feeling anxious; headaches; bloating; and muscle aches.
Similarly, the TV Ad “Balloons” starts by stating:
• “All birth control pills are 99% effective and can give you shorter, lighter periods. But there’s one Pill that goes beyond the rest. It’s YAZ.”
It then displays numerous balloons throughout the ad with symptoms, such as, “IRRITABILITY,” “MOODINESS,” “FEELING ANXIOUS,” “BLOATING,” “FATIGUE,” “MUSCLE ACHES,” “HEADACHES,” “INCREASED APPETITE,” and “ACNE.”
The symptoms displayed in these ads are commonly seen in women with PMS, which is a less serious and more common condition than PMDD. PMDD is a disorderwhose hallmarks include markedly depressed mood, anxiety or tension, affective lability, and persistent anger or irritability. Other features of PMDD include decreased interest in usual activities, difficulties concentrating, lack of energy, change in appetite or sleep, and feeling out of control. As discussed in the PI, for a diagnosis of PMDD:
… the disturbance markedly interferes with work or school, or with usual social activities and relationships with others. Diagnosis is made by healthcare providers according to the DSM-IV criteria, with symptomatology assessed prospectively over at least two menstrual cycles. In making the diagnosis, care should be taken to rule out other cyclical mood disorders.
The TV Ads entirely omit the material limitation from the PI of the drug’s PMDD indication – i.e., that “YAZ has not been evaluated for the treatment of premenstrual syndrome (PMS)” and fail to convey that the drug is only indicated for women who experience the symptomspresented to such a degree that they have PMDD, rather than PMS. As a result of the failure to convey these material facts, and the failure to explain what PMDD is, in contrast to PMS, the TV Ads misleadingly suggest that YAZ is approved to treat women with any severity of the symptoms presented, regardless of whether their symptoms are actually severe enough to constitute PMDD.
We note that the list of symptoms displayed in the TV Ads are accompanied by the text “YAZ treats PMDD” along with a SUPER reading “PMDD is a mood disorder related to the menstrual cycle.” However, these disclosures do not suffice to communicate the material fact that YAZ is not approved for treatment of PMS or to overcome the implication created by the totality of the visuals and images in the ads that YAZ is appropriate for any woman who experiences the symptoms presented. We also note that the voiceover states that “YAZ is the only birth control pill proven to treat the emotional and physical premenstrual symptoms that are severe enough to impact your life.” However, this claim also fails to communicate that YAZ is not approved for treatment of PMS, and fails to distinguish, between PMS and PMDD.
The totality of the visual and audio presentations in both TV ads suggest that YAZ is approved to treat women with any severity of the symptoms presented, including women with PMS, when this is not the case. Thus, the TV Ads misleadingly broaden the indication of the drug.
Acne
In addition, the TV Ads suggest that YAZ is approved for acne of all severities when this is not the case. Specifically, in “Not Gonna Take it,” the word “ACNE” appears in large print in the middle of the screen along with the audio claim “It can also help keep your skin clear,” which is accompanied bya close-up visual of a woman with completely clear skin. Similarly, in “Balloons,” the “ACNE” balloon is prominently displayed on the screen, as it floats by a smiling woman with obviously clear skin, along with the audio claim that YAZ ” … also helps keep skin clear.” These presentations fail to adequately convey that, as noted in the PI, “YAZ is indicated for the treatment of moderate acne vulgaris …” (emphasis added). While the TV Ads do include a SUPER which refers to “improvement in … moderate acne” in small, unbolded print, this does not mitigate the misleading impression created by the prominent audio and visual claims in the TV Ads that YAZ is indicated for acne of all severities. Overstatement of Efficacy
PMDD
“Balloons” (ZYRA-6567)
The TV Ad is misleading because it suggests that YAZ is more effective than has been demonstrated by substantial evidence or substantial clinical experience. The totality of the audio and visual claims and presentations misleadingly suggests that treatment with YAZ will allow women to say “good-bye” to their symptoms completely. For example, the TV Ad’s theme song “Good-Bye to you” plays in the background as energetic, euphoric, playful women release balloons into the air displaying certain symptoms (e.g., irritability, moodiness, feeling anxious, bloating, fatigue, muscle aches, headaches, increased appetite, and acne). The balloons then float up and away from the women misleadingly suggesting that these women are saying, ” goodbye” to their symptoms and are now symptom-free, when such an elimination of symptoms has not been demonstrated by substantial evidence or substantial clinical experience. According to the PI, in the primary clinical trial that served as the basis for approval of YAZ in the PMDD population, ” . . .the average decrease (improvement) from baseline was 37.5 points in women taking YAZ, compared to 30.0 points in women taking placebo” (added emphasis). These results do not support the implication that YAZ will result in a complete cessation of PMDD symptoms.
Acne
“Not Gonna Take It” (ZYRA-6323) & “Balloons” (ZYRA-6567)
The TV Ads include close-up images of women with completely clear, acne-free skin. In the TV Ad ” Not Gonna Take It,” there is an image of a woman with the word “ACNE” prominently displayed on the screen before the word “ACNE” fades away from view. The woman turns her face to the side showing viewers that she has no visible signs of acne on her face, in conjunction with the audio claim “It can also help keep your skin clear.” In “Balloons,” a woman with obviously clear skin smiles and acknowledges the ” ACNE” balloon as it floats away from the center of the screen and disappears into the sky, in conjunction with, the background song ” Good-bye to you” and the audio claim that YAZ ” . . .also helps keep skin clear.” The overwhelming impression conveyed by the TV Ads is that treatment with YAZ results in clear, acne-free skin for those women suffering from acne when this has not been demonstrated by substantial evidence or substantial clinical experience. As illustrated by Table III in the PI, the percentage of subjects assessed by the Investigator’s Static Global Assessment (ISGA) with a ‘clear’ or ‘almost clear’ rating at day 15 of cycle 6 was 15% and 21 % for subjects receiving YAZ versus 4% and 9% of placebo subjects in Studies 1 and 2, respectively. Furthermore, the mean percent reduction of total lesions at day 15 of cycle 6 was 42% and 46% for subjects receiving YAZ versus 25% and 31 % of placebo subjects in studies 1 and 2, respectively. Although these results are significant, they do not demonstrate that YAZ results in clear, acne-free skin for a typical woman; rather, these results demonstrate that it reduces the amount of acne lesions more than placebo but does not result in completely clear skin for these women. Thus, the TV Ads misleadingly overstate the efficacy of the drug.
Minimization of Risk
“Not Gonna Take It” (ZYRA-6323) & “Balloons” (ZYRA-6567)
The audio communication of serious risk disclosures during the “major statement” is minimized by distracting visuals, numerous scene changes, and other competing modalities such as the background music which combine to interfere with the presentation of the risk information. In “Not Gonna Take It”, the fast-paced visuals depict various women looking at pictures, trying on clothes, chatting at a cafe, stretching/exercising in a park, and walking down the street while the audio component describes the major risks associated with YAZ. Similarly, in “Balloons,” the background music plays as fast-paced visuals depict various women running in a park, sitting on a scenic waterfront, smiling, walking out of a coffee shop, driving and singing, walking out on a balcony, using an elevator, walking through the street to join friends, in addition, to a pigeon on a building ledge and balloons being released and floating away. These complex presentations distract from and make it difficult for viewers to process and comprehend the impo rtant risks being conveyed. This is particularly troubling as some of the risks being conveyed are serious, even life-threatening. The overall effect of the distracting visuals, graphics, concurrent supers and background music is to undermine the communication of important risk information, minimizing these risks and misleadingly suggesting that YAZ is safer than has been demonstrated by substantial evidence or substantial clinical experience.
Conclusion and Requested Action
For the reasons discussed above, the promotional piece misbrands YAZ in violation of the Act, 21 U.S.C. 352(n), 352(f)(1), & 321(n), and FDA implementing regulations. 21 CFR 201.1 00(c)(1); 201.128; 202.1 (e)(5)(iii) & 202.1(e)(6)(i).
DDMAC asks Bayer to immediately cease dissemination of violative promotional materials for YAZ that are the same as or similar to those described above. Please submit a written response to this letter on or before October 20, 2008, describing your intent to comply with this request, listing all promotional materials for YAZ that are the same as or similar to those described above, and explaining your plan for discontinuing use of such materials. Because the violations described above are serious, we request, further, that your submission include a comprehensive plan of action to disseminate truthful, non-misleading, and complete corrective messages about the issues discussed in this letter to the audience(s) that received the violative promotional materials. Please direct your response to me at the Food and Drug Administration, Center for Drug Evaluation and Research, Division of Drug Marketing, Advertising, and Communications, 5901-B Ammendale Road, Beltsville, MD 20705-1266, facsimile at (301) 847-8444. In all future correspondence regarding this matter, please refer to MACMIS ID # 16473 in addition to the NDA number(s). If you choose to revise your promotional materials, DDMAC is willing to assist you with your revised materials by commenting on your revisions before you use them in promotion. We remind you that only written communications are considered official.
The violations discussed in this letter do not necessarily constitute an exhaustive list. It is your responsibility to ensure that your promotional materials for YAZ comply with each applicable requirement of the Act and FDA implementing regulations. Failure to correct the violations discussed above may result in FDA regulatory action, including seizure or injunction, without further notice.
Sincerely,
{See appended electronic signature page}
Thomas Abrams, R.Ph., M.B.A.
Director
Division of Drug Marketing,
Advertising, and Communications
This is a representation of an electronic record that was signed electronically and this page is the manifestation of the elec tronic signature.
/s/
Thomas Abrams
10/3/2008 04:31:08 PM