Serious side effects of Aldara are unusual but may happen. Buy aldara cream online For example, Aldara may, in some circumstances, cause severe discomfort or soreness which could be indicative of a severe skin reaction. If this is the case, you will notice symptoms such as:
If you have been taking Aldara to treat genital warts, and you are concerned that any reactions or side effects you are experiencing are abnormal (particularly if they persist or worsen), then you should consult your doctor for further guidance.
You may need to stop the treatment to give your skin time to recover, but it is best to talk to your doctor or pharmacist as this could impact the effectiveness of the treatment.
Tell your doctor straight away if any of these unlikely but serious side effects occur and persist:
In very rare cases, users may suffer from an allergic reaction — we will cover these symptoms in the ‘Possible allergic reactions’ section below.
Aldara, Zyclara Cream should be applied 2 times per week for a full 16 weeks to a defined treatment area on the face or scalp (but not both concurrently). Before applying the cream, the patient should wash hands and the treatment area with mild soap and water and allow the area to dry thoroughly. Avoid contact with eyes, lips and nostrils.
The dermatologist scrapes or shaves off the BCC using a curette (a sharp instrument with a ring-shaped tip), then uses heat or a chemical agent to destroy remaining cancer cells, stop the bleeding and seal off the wound. The physician may repeat the procedure a few times during the same session until no cancer cells remain. Typically, the procedure leaves a round, whitish scar resembling a cigarette burn at the surgery site.
The data described below reflect exposure to Imiquimod Cream or vehicle in 479 subjects enrolled in two double-blind, vehicle-controlled trials. http://healthquestions.medhelp.org/aldara-alternatives Subjects applied up to two packets of Imiquimod Cream or vehicle daily to the skin of the affected area (either entire face or balding scalp) for two 2-week treatment cycles separated by a 2-week no-treatment period.
Application site pruritus
1 ( Table 2: Local Skin Reactions in the Treatment Area in Imiquimod-Treated Subjects as Assessed by the Investigator (AK) All Grades (%) Severe (%) Imiquimod Cream, 3.75% (N=160) Imiquimod Cream, 2.5% (N=160) Vehicle (N=159)
Erythema Severe erythema
Scabbing/Crusting Severe scabbing/crusting
Edema Severe edema
Erosion/Ulceration Severe erosion/ulceration
Exudate Severe exudate
Flaking/Scaling/Dryness Severe flaking/scaling/dryness
Overall, in the clinical trials, 11% (17/160) of subjects in the Imiquimod Cream, 3.75% arm, 7% (11/160) of subjects in the Imiquimod Cream, 2.5% arm, and 0% in the vehicle cream arm required rest periods due to adverse local skin reactions.
Other adverse reactions observed in subjects treated with Imiquimod Cream include: application site bleeding, application site swelling, chills, dermatitis, herpes zoster, insomnia, lethargy, myalgia, pancytopenia, pruritus, squamous cell carcinoma, and vomiting.
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