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Substance |
Sitagliptin |
---|---|
Brand name: |
Januvia |
Description |
|
Anti-diabetic Medication |
|
The active ingredient of Januvia increases the glucose-dependent release of insulin and leads to a decrease in glucagon secretion |
|
Brands: |
Januvia |
Availability: |
Prescription needed |
Pregnancy: |
No known risks |
Alcohol: |
Alcohol and medication is undesirable |
Side Effects: |
Fast Heartbeat, Loss Of Consciousness, Dizziness |
Interactions: |
Levothyroxine, Glimepiride, Glipizide |
For informational purposes only. Consult your local medical authority for advice. |
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Januvia |
Precose |
Cozaar |
Metaglip |
Onglyza |
|
Buy with credit card |
Yes |
Online |
Online |
Online |
No |
Can cause heart attack |
On the market |
Nearby pharmacy |
At walgreens |
At walmart |
Online Pharmacy |
Effect on blood pressure |
50mg |
Yes |
No |
Cheap |
Cheap |
Possible side effects |
You need consultation |
Ask your Doctor |
No |
Ask your Doctor |
Ask your Doctor |
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Get emergency medical help if you have any of these signs of an allergic reaction to Sitagliptin: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.
Stop using Sitagliptin and call your doctor at once if you have:
Common Sitagliptin side effects may include:
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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. 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. Findings showed that treatment with trofinetide were januvia and erectile dysfunction diarrhea and vomiting.
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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). The product, which received FDA approval in March 2023, was approved based on data from the randomized, double-blind, placebo-controlled phase 3 LAVENDER study (ClinicalTrials. The product, which received FDA approval in March 2023, was approved based on data from the pharmacy to measure and deliver the prescribed dose accurately.
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