There are no studies using Botox in pregnant women. In animal studies, Botox administration resulted in adverse effects on fetal growth (decreased fetal weight and skeletal ossification).

Tell your health care provider if you are taking blood thinners or medicines that can interfere with the clotting of blood, such as aspirin or warfarin. These medicines might make it more likely that you will experience bruising or bleeding at the injection site.

Depending on patient symptoms, institute catheterization if PVR urine volume exceeds 200 mL and continue until PVR falls below 200 mL. Instruct patients to contact their physician if they experience difficulty in voiding as catheterization may be required.

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.

For some, it can take up to 30 days to see the full effects after getting Botox Cosmetic injections. Many injectors schedule follow-up appointments within the first few weeks to evaluate the results.

Repeat injections for hyperhidrosis should be administered when the clinical effect of a previous injection diminishes.

Check out these common questions for more info about Radiesse and what your patients can expect from treatment.

Delayed-onset inflammation near the sitio of injection is one of the known adverse events associated with dermal fillers. Cases of delayed-onset inflammation have been reported to occur at the treatment site following viral or bacterial illnesses or infections, vaccinations, or dental procedures. Typically, the reported inflammation was responsive to treatment or resolved on its own.

Other common side effects experienced by those being treated with Botox for urinary incontinence are:

Patients with smaller neck muscle mass and patients who require bilateral injections into the sternocleidomastoid muscle for the treatment of cervical dystonia have been reported to be at greater risk for dysphagia.

In several of the cases, patients had pre-existing dysphagia or other significant disabilities. There is insufficient information to identify factors associated with an increased risk for adverse reactions associated with the unapproved uses of BOTOX. The safety and effectiveness of BOTOX for unapproved uses have not been established.

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Injection in the back of the hand may result in temporary difficulty performing activities. radiesse RADIESSE® may cause nodules, bumps or lumps in the back of the hand and can last up to 1 year.

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.