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Stevens Johnson Syndrome Changing People's Lives

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DeKalb, IL: Many people do not know that when they take common medications, they could be putting themselves at risk of Stevens Johnson Syndrome. Also known as SJS, Stevens Johnson Syndrome is a potentially fatal disease that often has serious consequences even for patients who survive their Stevens Johnson Syndrome skin disease. Unfortunately, many patients who develop the disease are children and youth, and even after they recover from their ordeal, they have permanent injuries to deal with.

Stevens Johnson Syndrome Changing People's LivesMSNBC (04/20/11) reports the case of Veronica Zenkner, who, at age 13, took two ibuprofen over two days to relieve a headache. Zenkner developed Stevens Johnson Syndrome and suffered from a rash and fever. She went to the hospital where she was diagnosed with toxic epidermal necrolysis—a more serious form of SJS in which the patient suffers blisters on more than 30 percent of his or her body. Zenkner was reportedly put in a medically induced coma.

Luckily, Zenkner survived her ordeal. But now, seven years after her battle with SJS, she is blind in one eye, has permanent scarring and still has a patch on her head where her hair did not grow back.

SJS is an allergic reaction to medication. What makes it so concerning is that it can appear at any time, even after a patient has taken the same medication for years with no signs of side effects. And, although certain medications such as anti-inflammatory drugs are more highly linked to Stevens Johnson Syndrome, just about any drug could cause the allergic reaction. Because SJS is not well known or well documented, patients are often misdiagnosed or continue taking the medication that caused the reaction, not realizing the harm that is being done.

Furthermore, although some medications warn specifically about the risk of SJS, others only warn about the risk of a severe allergic reaction—but do not name SJS or mention specifically how devastating the allergic reaction can be.

And for some patients, it is devastating. SJS can cause blistering of the skin and mucous membranes. In some patients, the skin sloughs off in sheets, leaving the patient vulnerable to infections. Some patients suffer permanent eye damage, including blindness. Others may retain some of their eyesight but become photosensitive, meaning they cannot be out in the light without protection on their eyes.

In some situations, the patient may not be aware that he or she has been put at risk of Stevens Johnson Syndrome until it is too late. In March, a teenager on a flight to California suffered an aneurism. After a first open-heart surgery, doctors discovered the patient would require a second open-heart surgery. Following that second surgery, the teen developed Stevens Johnson Syndrome, suffering blisters all over his skin and putting him into a coma.

According to the Ledger-Enquirer (04/17/11), surgery to save the teen's vision went well, but the results of that surgery are not yet known for certain.

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READER COMMENTS

Posted by
jose
on
I was hospitalized (3rd time 6 mos. after my 6 heart bypass surgery) because of severe chest pain. I developed fever,chills when I was at the hospital and was given Sulindac (Clinoril), Gentamicin, Ceftizoxime, Tylinol and several more medications. Doctors said that I had an OCCULT INFECTION and I was placed on empiric antibiotics for 24 hours. Then again I developed a faint erythematous pretibial rash, headache, sore throat, sweating. Antibiotics were switched to Nafcillin which I had an allergic reactions :1) an inflamed pancreas 2) angioedema almost of my entire body ,my eyes, tongue, throat, lips were all swollen. The pretibial rash became more prominent during the day and I was diagnosed of CELLULITIS. After my discharge, more blisters and rashes grew more up to the left and right groin and my entire organ area, down to the anal area. I went to see a dermatologist and told him of the diagnosis (never did a culture) and prescribed me a cream and a solution of .05% Flucinonide. Then I was prescribed Vioxx for years and switched to Sulindac for more years and my CELLULITIS was getting worse and worse. I did a research about CELLULITIS 'coz I want to get the best cure and then I found out that CELLULITIS was caused by Staph Aureus bacteria. I went back to my medical records and found out that blood and urine cultures were negative of any bacterial growth. I made comparison between CELLULITIS and SJS and then contacted the doctor who diagnosed my cellulitis and asked him if I really had cellulitis or SJS (I faxed him my medical records) and advised me to just ask my present physician (through his nurse). I even told him that I'm not suing him but I just want his real diagnosis and the real disease that I suffered but he doesn't even want to talk to me. Several attempts to contact him but no response at all. My present physician said that he can't reverse someone's diagnosis but instead he changed my medication (Flucinonide w/c I used it for almost 10 yrs.). I am still looking forward to find out if i really had an SJS.

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