Why patients develop Stevens Johnson Syndrome is not fully understood. What is known is that the condition is a very rare, yet severe, allergic reaction to medications. The condition often starts as a painful rash, sometimes with blisters. By the time the patient is diagnosed, his skin may start sloughing off, exposing large areas of flesh.
In addition to losing the outer layer of skin, patients may also experience sloughing of their mucous membranes and of the lining of their internal organs. Those who survive their experiences often have permanent scarring, damage to their eyesight and damage to their tear ducts.
Some patients fall into a coma. Some die from their injuries.
Patients may have no idea they are allergic to the medication until the reaction occurs. People have developed Stevens Johnson Syndrome after taking a wide variety of medications, including medications as seemingly harmless as headache remedies.
READ MORE STEVENS JOHNSON SYNDROME (SJS) LEGAL NEWS
One patient who survived her ordeal is Kendra Schmidt, who developed SJS two years ago after taking a prescription medication. According to the News-Record on 7/30/10, Schmidt was in the hospital for two to two and a half months. She required pig skin for a graft because she did not have any viable skin. Schmidt has a prosthetic over one eye and a special lens over the other eye. She does not have fingernails and has broken her toe three times since her ordeal.
READER COMMENTS
Subhash Gupta
on