Carniwell Tablet belongs to the class of 'nutraceutical products', primarily used to treat carnitine deficiency. Carnitine deficiency is a metabolic muscle disease caused by low levels of carnitine. Carnitine is an amino acid that helps in the production of energy from fatty acids. Symptoms of carnitine deficiency include weakness in the muscles of hips, shoulders, upper arms and legs, low blood sugar, fatigue, vomiting, abdominal pain, growth retardation and low weight.

Carniwell Tablet contains L-Carnitine or Levo-carnitine, a naturally occurring derivative of the amino acids, lysine and methionine. When taken as a supplement, the body converts L-Carnitine into acetyl-L-carnitine and propionyl-L-carnitine. These products further help the body to produce energy from fat.

Your doctor will decide the dosage based on your medical condition. Sometimes, Carniwell Tablet may have common side effects like stomach pain, nausea, vomiting, and diarrhoea. These side effects do not require medical attention and gradually resolve over time. However, if these side effects persist for a longer time, please seek medical advice.

Let your doctor know if you are using suggested, non-suggested drugs and herbal products before starting Carniwell Tablet . If you are known to be allergic to Carniwell Tablet or its inactive components, please inform your doctor. Please tell your doctor if you have an underactive thyroid (hypothyroidism), liver or kidney diseases, diabetes, fits, and dialysis treatment. If you are a pregnant or breastfeeding mother, please consult your doctor before taking Carniwell Tablet . Carniwell Tablet is not recommended for children under 12 years of age.

Carniwell Tablet is used to treat primary and secondary carnitine deficiency. It contains L-Carnitine or Levo-carnitine, a naturally occurring derivative obtained from amino acids, lysine and methionine. When the body lacks the carnitine, Carniwell Tablet helps in replacing those low levels. Carniwell Tablet is further converted into acetyl-L-carnitine and propionyl-L-carnitine in the body. These products further help the body to produce energy from fat. Carniwell Tablet also plays a role as a water-soluble vitamin, antilipemic drug (lowers blood cholesterol), and a nootropic agent (improve cognitive function).

• Stomach pain
• Nausea
• Vomiting
• Diarrhoea 

Let your doctor know if you are using suggested, non-suggested drugs, and herbal products before starting Carniwell Tablet . Inform your doctor if you are allergic to Carniwell Tablet or its inactive components. Please inform your doctor if you have underactive thyroid (hypothyroidism), liver or kidney diseases, diabetes, and fits. Inform your doctor if you need to undergo dialysis treatment before starting Carniwell Tablet . Pregnant or breastfeeding women should consult their doctor before taking Carniwell Tablet . Keep Carniwell Tablet away from direct sunlight. Do not store Carniwell Tablet above 25°C and keep it away from direct sunlight.

Drug-Drug Interaction: Carniwell Tablet may interact with blood thinners (warfarin, acenocoumarol).

Drug-Food Interaction: No interactions found/established.

Drug-Disease Interaction: Use Carniwell Tablet with medical advice if you have an underactive thyroid (hypothyroidism), liver or kidney diseases, diabetes, fits, and allergic reactions to medicines.

• WARFARIN
• ACENOCOUMAROL

• Try food sources like milk, cheese, eggs, liver and kidney, chicken, red meat, tuna, mackerel, and salmon, shellfish, oysters, clams, dark green vegetables, such as spinach and kale, beets, avocados, and potatoes, whole grains, cereals, kidney beans, black beans, and chickpea.
• Include fruits like citrus, banana, and watermelon in your diet.
• Avoid smoking and alcohol consumption.
• Exercise regularly and maintain a healthy lifestyle. 
• Avoid excess fatty foods.

Let your doctor and the laboratory staff know if you are using Carniwell Tablet since it may interfere with laboratory tests. 

Carnitine deficiency is a metabolic muscle disease caused by low levels of carnitine. Carnitine is an amino acid that helps in the production of energy from fatty acids. Carnitine deficiency can be primary and secondary. Primary carnitine deficiency occurs due to a genetic mutation in the substance responsible for bringing the carnitine into the cells. Secondary carnitine deficiency occurs when there is not enough carnitine in the blood. Symptoms of carnitine deficiency include weakness in the muscles of hips, shoulders, upper arms, and legs, low blood sugar, fatigue, vomiting, abdominal pain, growth retardation, and low weight.