Devita Injection is used to treat or prevent some complications associated with long-term kidney dialysis, such as low calcium levels (Hypocalcaemia). Hypocalcaemia is characterized by low levels of calcium in the blood. A lack or inadequacy of vitamin D can cause hypocalcaemia.

Devita Injection contains calcitriol. It increases the levels of vitamin D in your blood, which in turn raises calcium levels thus, it helps to treat patients with low levels of calcium who are on chronic renal dialysis.

Devita Injection is given by a health care professional in a hospital or clinic setting. In some cases, Devita Injection can cause side effects like Nausea, headache, constipation, or pain/discomfort at the injection site may occur. Most of these side effects of Devita Injection do not require medical attention and gradually resolve over time. However, if these side effects persist longer, please consult your doctor.

Before taking the Devita Injection, let your doctor know about all your medical conditions, sensitivities, and medications you are using. Inform your doctor if you have too much calcium or vitamin D in the blood before receiving the Devita Injection. Also, inform your doctor if you are pregnant, planning to become pregnant, or breastfeeding.

Devita Injection contains calcitriol. It increases the levels of vitamin D in your blood, which raises calcium levels; thus, it helps treat patients with low levels of calcium who are on chronic renal dialysis. Calcitriol is usually used along with a certain diet, supplements, and sometimes other medications. It can also help to build and keep strong bones.

• Nausea
• Headache
• Constipation or upset stomach
• Loss of appetite
• Dry mouth
• Pain/discomfort at the injection site

Before taking the Devita Injection, let your doctor know about all your medical conditions, sensitivities, and all medications you are using. Inform your doctor if you are with malabsorption syndrome (difficulty absorbing nutrition from food) or if you are diagnosed with too much calcium or vitamin D in the blood before receiving the Devita Injection. Devita Injection should not be used for pregnant and lactation mothers unless clearly necessary. So, inform your doctor if you are a pregnant woman or a nursing mother. Your doctor will weigh the benefits and potential risks before prescribing Devita Injection.

Drug-Drug interactions: Devita Injection may interact with medications used for the treatment of Tumor-Induced Osteomalacia (e.g. burosumab), cardiac glycosides (e.g. digoxin, digitalis), magnesium-containing medications (e.g. milk of magnesia), vitamins/nutritional supplements (e.g. calcium and vitamin D) and phosphate binders (e.g. sevelamer).

Drug-Food interactions: Do not take foods enriched with vitamin D and avoid a high intake of dairy products such as milk, ghee, and cheese.

Drug-Disease interactions: Devita Injection may interact with various disease conditions, including hypercalcemia (high levels of calcium in the blood), metastatic calcification (extra deposits of calcium in the body), kidney problems, heart problems and high levels of vitamin D; so inform your doctor about your medical condition.

• Burosumab
• DIGOXIN
• DIGITALIS
• MILK OF MAGNESIA
• CALCIUM
• VITAMIN D
• SEVELAMER

• Include dairy products like milk, yoghurt, cheese, or milk-based custard in your diet.

• Eat a serving of broccoli, cabbage, bok choy, spinach, and other green leafy vegetables daily.

• Snack on calcium-rich nuts like Brazil nuts or almonds.

• Sprinkle sesame seeds over your food, vegetables, and salads. Sesame seeds are high in calcium.

• Avoid or reduce the intake of caffeine, soft drinks, and alcohol that inhibit calcium absorption.

• Replace the meat with tofu or tempeh for extra calcium in your food.

Hypocalcaemia: Low calcium levels in the blood are referred to as hypocalcaemia. It is most usually caused by vitamin D insufficiency or hypoparathyroidism.