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|---|---|---|---|
| January | Caribbean Dermatology | January 15-19 | St. Thomas, VI |
| Orlando Dermatology | January 18-20 | Orlando, FL | |
| February | American Academy of Dermatology Winter Meeting | February 1-5 | San Antonio, TX |
| March | Hawaii Dermatology | March 1-7 | Waikoloa, HI |
| AOCD Mid-Year Meeting | March 12-15 | Monterey, CA | |
| Winter Clinical | March 14-18 | Maui, HI | |
| April | Derm Foundation | April 2-6 | Amelia Island, FL |
| May | |||
| June | Alabama Derm | June 28-30 | Sandestin, FL |
| July | Alabama Derm | July 1 | Sandestin, FL |
| American Academy of Dermatology Summer Meeting | July 30-31 | Chicago, IL | |
| August | American Academy of Dermatology Summer Meeting | August 1-3 | Chicago, IL |
| September | |||
| October | Fall Clinical | October 18-21 | Las Vegas, NV |
| AOCD Annual Meeting | October 26-30 | Las Vegas, NV | |
| November | SDPA | November 4-8 | Tampa Bay, FL |
| December |
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TAZORAC® (tazarotene) Cream 0.1% is indicated for acne vulgaris. Contraindications Retinoids may cause fetal harm when administered to a pregnant woman. TAZORAC® Cream and Gel 0.1% are contraindicated in women who are or may become pregnant. If this drug is used during pregnancy, or if the patient becomes pregnant while taking this drug, treatment should be discontinued and the patient apprised of the potential hazard to the fetus. WarningsWomen of child-bearing potential should be warned of the potential risk and use adequate birth-control measures when TAZORAC® Cream or Gel 0.1% is used. PrecautionsRetinoids should not be used on eczematous skin, as they may cause severe irritation. TAZORAC® Cream or Gel 0.1% should be administered with caution if the patient is also taking drugs known to be photosensitizers (e.g., thiazides, tetracyclines, fluoroquinolones, phenothiazines, sulfonamides) because of the increased possibility of augmented photosensitivity. Adverse ReactionsThe most frequent adverse reactions reported during clinical trials with TAZORAC® Cream 0.1% in the treatment of acne occurring in 10% to 30% of patients, in descending order, included desquamation, dry skin, erythema, and burning sensation. The most frequent adverse events reported with TAZORAC® Gel 0.1% in the treatment of acne occurring in 10% to 30% of patients, in descending order, included desquamation, burning/stinging, dry skin, erythema, and pruritus. Please click here for full prescribing information for TAZORAC® Cream and Gel 0.1%. |
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