Orlistat

Brand name: Xenical

Description

Weight Loss Medication
Along with a low-calorie diet it has been found to reduce your obesity and discourage the return of unwanted pounds
Brands: Xenical And Alli
Availability: Prescription needed
Pregnancy: Consult a doctor
Alcohol: Not detected with light alcohol consumption
Side Effects: Loss Of Voice, General Feeling Of Discomfort Or Illness, Fast Heartbeat
Interactions: Vitamin D3 (cholecalciferol), Levothyroxine, Metformin
For informational purposes only. Consult your local medical authority for advice.

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Since orlistat can cause decreased absorption of some fat-soluble vitamins, you may need to take a daily multivitamin that contains normal amounts of vitamins D, E, K and beta-carotene. Take the multivitamin once per day at least 2 hours after your dose of orlistat unless otherwise directed by your physician or other healthcare professional. Watch for any unusual changes in your body's normal function. You need to watch the amount of fat in your diet. Too much dietary fat can increase the side effects from orlistat. Also, watch for any changes in your eyesight, skin or hair that may be caused by a vitamin deficiency.

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Having a therapy that has been shown to address multiple symptoms of Rett syndrome provides a promising treatment option that may lead to meaningful impact for patients and their families. The most common adverse reactions reported with trofinetide were diarrhea and vomiting. Rett syndrome provides a promising treatment option that may lead to meaningful impact for patients and their families.

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A calibrated measuring device (eg, oral syringe, oral dosing cup) should be obtained from the randomized, double-blind, placebo-controlled phase 3 LAVENDER study (ClinicalTrials. Findings showed that treatment with trofinetide led to statistically significant improvements on the Rett Syndrome Behaviour Questionnaire total score and the Clinical Global Impression-Improvement score at week 12 compared with placebo (coprimary endpoints). Findings showed that treatment with trofinetide led to statistically significant improvements on the Rett Syndrome Behaviour Questionnaire total score and the Clinical Global Impression-Improvement score at week 12 compared with placebo (coprimary endpoints).