O guia definitivo para radiesse
O guia definitivo para radiesse
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An injection of BOTOX is prepared by drawing into an appropriately sized sterile syringe an amount of the properly reconstituted toxin slightly greater than the intended dose.
Tell your doctor if you are pregnant, intending to become pregnant, or breastfeeding before being administered Botox because it may not be suitable for you.
Repeat injections for hyperhidrosis should be administered when the clinical effect of a previous injection diminishes.
Subsequent injections should not be administered until the effects of the previous dose have dissipated as evidenced by substantial function in the injected and adjacent muscles.
Based on animal data, onabotulinumtoxinA may harm your unborn baby. Talk to your healthcare provider about the risks of receiving this medicine during pregnancy.
Patients should discontinue anti-platelet therapy at least 3 days before the injection procedure. Patients on anti-coagulant therapy need to be managed appropriately to decrease the risk of bleeding. Appropriate caution should be exercised when performing a cystoscopy.
Since onabotulinumtoxinA has a temporary effect and is given at widely spaced intervals, missing a dose is not likely to be harmful.
OnabotulinumtoxinA may cause loss of strength or general muscle weakness, vision problems, or dizziness within hours to weeks of receiving Botox or Botox Cosmetic. If this happens, do not drive a car, operate machinery, or do other dangerous activities.
Botox Cosmetic is used for aesthetic purposes to smooth wrinkles and improve the appearance of platysma bands.
You should not use RADIESSE® or RADIESSE® (+) if you have an allergy to any component of the product, if you have a history of severe allergies, if you have a bleeding disorder, or if you are pregnant or breastfeeding. You should not use RADIESSE® (+) if you have an allergy to lidocaine or medicines like it.
Please see the Patient Information Guide available at for list of these events. Tell your health care provider about any side effects that bother you or do not go away.
Must be administered by a licensed provider and reconstituted exactly as directed by the manufacturer.
Injection in the back of the hand may result in temporary difficulty performing activities. RADIESSE® may cause nodules, bumps or lumps in the back of the hand and can last up to 1 year.
Because clinical trials are conducted under widely varying conditions, the adverse reaction rates observed in the clinical trials of a bioestimulador de colágeno drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice.