NEUTRON OD TABLET

Manufacturer :
Composition : MECOBALAMIN-1000MCG+BENFOTIAMINE-100MG+L METHYLFOLATE-300MCG+ZINC-15MG+CHROMIUM-65MCG+MAGNESIUM-15MG+CHOLINE CHLORIDE-30MCG+IODINE-150MCG+CALCIUM CARBONATE-162MG+MANGANESE-1.4MG+ALPHA LIPOIC ACID-100MG
Dose Form : TABLET
Description : NEUTRON OD TAB
Route Of Administration : ORAL
Pack : 10
Out of stock
SKU
NEU0087
₹139.00
Manufacturer :
Composition : MECOBALAMIN-1000MCG+BENFOTIAMINE-100MG+L METHYLFOLATE-300MCG+ZINC-15MG+CHROMIUM-65MCG+MAGNESIUM-15MG+CHOLINE CHLORIDE-30MCG+IODINE-150MCG+CALCIUM CARBONATE-162MG+MANGANESE-1.4MG+ALPHA LIPOIC ACID-100MG
Dose Form : TABLET
Description : NEUTRON OD TAB
Route Of Administration : ORAL
Pack : 10

Drug Ingredient Information

MECOBALAMIN-1000MCG+BENFOTIAMINE-100MG+L METHYLFOLATE-300MCG+ZINC-15MG+CHROMIUM-65MCG+MAGNESIUM-15MG+CHOLINE CHLORIDE-30MCG+IODINE-150MCG+CALCIUM CARBONATE-162MG+MANGANESE-1.4MG+ALPHA LIPOIC ACID-100MG

MECOBALAMIN

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Drug Pregnancy Interaction
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How to take the Medicine
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Drug quanitty
Drug Dose
Excess Drug Consumption
Forgot Drug Consumption
Stop Drug Consumption
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Common Drug Side Effects
Rare Drug Side Effects
Very Rare Drug Side Effects
Drug Side Effects Symptoms
How to Store the Medicine
How to Store the Medicine

BENFOTIAMINE

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Drug Information
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Alert
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Avoid Drug
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Drug Pregnancy Interaction
Drug Breast feeding Interaction
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Drug Dose
Excess Drug Consumption
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Stop Drug Consumption
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General Information
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Rare Drug Side Effects
Very Rare Drug Side Effects
Drug Side Effects Symptoms
How to Store the Medicine
How to Store the Medicine

L METHYLFOLATE

Information for patients
Drug Information Dietary management of low plasma or low red blood cell folate in certain patients. It may also be used for other conditions as determined by your doctor. L-Methylfolate is a medical food. It works by providing the body with folate.
Drug Alert
Alert Some brands of L-Methylfolate may contain tartrazine dye (FD&C Yellow No. 5). This may cause an allergic reaction in some patients. If you have ever had an allergic reaction to tartrazine, ask your pharmacist if your product has tartrazine in it. Lab tests, including blood counts, may be performed while you use L-Methylfolate. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments. L-Methylfolate should be used with extreme caution in CHILDREN; safety and effectiveness in children have not been confirmed. PREGNANCY and BREAST-FEEDING: It is not known if L-Methylfolate can cause harm to the fetus. If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using L-Methylfolate while you are pregnant. L-Methylfolate is found in breast milk. If you are or will be breast-feeding while you use L-Methylfolate, check with your doctor. Discuss any possible risks to your baby.
Before Consuming the Medicine
Avoid Drug you are allergic to any ingredient in L-Methylfolate Contact your doctor or health care provider right away if any of these apply to you.
Drug Special Care Some medical conditions may interact with L-Methylfolate. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you: if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances if you have anemia or low levels of vitamin B12 in the blood Some MEDICINES MAY INTERACT with L-Methylfolate. Tell your health care provider if you are taking any other medicines, especially any of the following: Cholestyramine, colchicine, colestipol, nonsteroidal anti-inflammatory drugs (NSAIDs) (eg, ibuprofen), or sulfasalazine because they may decrease L-Methylfolate's effectiveness Fluorouracil because the risk of its side effects may be increased by L-Methylfolate Barbiturates (eg, phenobarbital), carbamazepine, hydantoins (eg, phenytoin), primidone, or valproic acid because they may decrease L-Methylfolate's effectiveness; their effectiveness may also be decreased by L-Methylfolate Pyrimethamine because its effectiveness may be decreased by L-Methylfolate This may not be a complete list of all interactions that may occur. Ask your health care provider if L-Methylfolate may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.
Drug Drug Interactions no data available
Drug Pregnancy Interaction It is not known if L-Methylfolate can cause harm to the fetus. If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using L-Methylfolate while you are pregnant.
Drug Breast feeding Interaction L-Methylfolate is found in breast milk. If you are or will be breast-feeding while you use L-Methylfolate, check with your doctor. Discuss any possible risks to your baby.
Drug Machinery Interaction no data available
Drug More Information no data available
How to take the Medicine
Consumption Info L-methylfolate is only part of a complete program of treatment that may also include other medications, and psychological counseling when used in people with depression or schizophrenia. Follow your medication and counseling routines very closely.
Drug quanitty Take one (1) tablet daily with food,
Drug Dose Use L-Methylfolate as directed by your doctor. Check the label on the medicine for exact dosing instructions. Take L-Methylfolate by mouth with or without food. If you miss a dose of L-Methylfolate, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once. Ask your health care provider any questions you may have about how to use L-Methylfolate.
Excess Drug Consumption Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately.
Forgot Drug Consumption Contact Your doctor
Stop Drug Consumption Do not stop the drug untill your doctor says you to do so.
Possible Side Effects
General Information no data available
Common Drug Side Effects All medicines may cause side effects, but many people have no, or minor, side effects. No COMMON side effects have been reported with L-Methylfolate. Seek medical attention right away if any of these SEVERE side effects occur: Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue). This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency,
Rare Drug Side Effects no data available
Very Rare Drug Side Effects no data available
Drug Side Effects Symptoms An overdose of l-methylfolate is not likely to cause life-threatening symptoms.
How to Store the Medicine
How to Store the Medicine Store L-Methylfolate at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store in original container until just before use. Store away from heat, light, and moisture. Do not store in the bathroom. Keep L-Methylfolate out of the reach of children and away from pets.

ZINC

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Alert
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Drug Pregnancy Interaction
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Drug quanitty
Drug Dose
Excess Drug Consumption
Forgot Drug Consumption
Stop Drug Consumption
Possible Side Effects
General Information
Common Drug Side Effects
Rare Drug Side Effects
Very Rare Drug Side Effects
Drug Side Effects Symptoms
How to Store the Medicine
How to Store the Medicine

CHROMIUM

Information for patients
Drug Information Treating or preventing chromium deficiency. Chromium Picolinate is a mineral. It works by increasing the blood levels of chromium.
Drug Alert
Alert
Before Consuming the Medicine
Avoid Drug • Diabetes patients - Chromium Picolinate may affect your blood sugar. Check blood sugar levels closely and ask your doctor before adjusting the dose of your diabetes medicine. • PREGNANCY and BREAST-FEEDING: If you become pregnant, discuss with your doctor the benefits and risks of using Chromium Picolinate during pregnancy. If you are or will be breast-feeding while you are using Chromium Picolinate, check with your doctor or pharmacist to discuss the risks to your baby. • you are allergic to any ingredient in Chromium Picolinate Contact your doctor or health care provider right away if any of these apply to you.
Drug Special Care Some medical conditions may interact with Chromium Picolinate. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you: • if you are pregnant, planning to become pregnant, or are breast-feeding • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement • if you have allergies to medicines, foods, or other substances Some MEDICINES MAY INTERACT with Chromium Picolinate. However, no specific interactions with Chromium Picolinate are known at this time. This may not be a complete list of all interactions that may occur. Ask your health care provider if Chromium Picolinate may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.
Drug Drug Interactions no data available
Drug Pregnancy Interaction : If you become pregnant, discuss with your doctor the benefits and risks of using Chromium Picolinate during pregnancy
Drug Breast feeding Interaction . If you are or will be breast-feeding while you are using Chromium Picolinate, check with your doctor or pharmacist to discuss the risks to your baby.
Drug Machinery Interaction no data available
Drug More Information no data available
How to take the Medicine
Consumption Info no data available
Drug quanitty no data available
Drug Dose How to use Chromium Picolinate: Use Chromium Picolinate as directed by your doctor. Check the label on the medicine for exact dosing instructions. • Take Chromium Picolinate with food. • Take Chromium Picolinate with a full glass of water (8 oz/240 mL). • If you miss taking a dose of Chromium Picolinate for 1 or more days, there is no cause for concern. If your doctor recommended that you take it, try to remember your dose every day. Ask your health care provider any questions you may have about how to use Chromium Picolinate.
Excess Drug Consumption Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include kidney or liver damage; loss of consciousness; seizures; upset stomach; vomiting.
Forgot Drug Consumption Contact Your doctor
Stop Drug Consumption Do not stop the drug untill your doctor says you to do so.
Possible Side Effects
General Information no data available
Common Drug Side Effects All medicines may cause side effects, but many people have no, or minor, side effects. When used in small doses, no COMMON side effects have been reported with this product. Seek medical attention right away if any of these SEVERE side effects occur:Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue).This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency,
Rare Drug Side Effects no data available
Very Rare Drug Side Effects no data available
Drug Side Effects Symptoms no data available
How to Store the Medicine
How to Store the Medicine Store in a cool and dry place.

MAGNESIUM

Information for patients
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Drug Dose
Excess Drug Consumption
Forgot Drug Consumption
Stop Drug Consumption
Possible Side Effects
General Information
Common Drug Side Effects
Rare Drug Side Effects
Very Rare Drug Side Effects
Drug Side Effects Symptoms
How to Store the Medicine
How to Store the Medicine

CHOLINE CHLORIDE

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Drug Information
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Drug Dose
Excess Drug Consumption
Forgot Drug Consumption
Stop Drug Consumption
Possible Side Effects
General Information
Common Drug Side Effects
Rare Drug Side Effects
Very Rare Drug Side Effects
Drug Side Effects Symptoms
How to Store the Medicine
How to Store the Medicine

IODINE

Information for patients
Drug Information Pre-operative reduction of vascularity of the thyroid gland Grave's disease in neonates Radiation protection against radioactive iodine Cutaneous or lymphocutaneous sporotrichosis Iodine deficiency disorders Thyroid storm
Drug Alert
Alert no data available
Before Consuming the Medicine
Avoid Drug Hypersensitivity. Acute bronchitis (potassium iodide).
Drug Special Care Children. Adult >45 yr. Topical applications should not be covered with occlusive dressings. Nodular goitre. Renal impairment. Hypocomplemetemic vasculitis. TB (potassium iodide). Pregnancy and lactation.
Drug Drug Interactions Additive or synergistic hypothyroid effect with lithium salts, antithyroid agents. Additive hyperkalaemia with combined use of potassium iodide and potassium-containing drugs or potassium-sparing diuretics.
Drug Pregnancy Interaction Category D: There is positive evidence of human foetal risk, but the benefits from use in pregnant women may be acceptable despite the risk (e.g., if the drug is needed in a life-threatening situation or for a serious disease for which safer drugs cannot be used or are ineffective).
Drug Breast feeding Interaction no data available
Drug Machinery Interaction no data available
Drug More Information no data available
How to take the Medicine
Consumption Info no data available
Drug quanitty Pre-operative reduction of vascularity of the thyroid gland Adult: As potassium iodide: 50-250 mg (approx 1-5 drops of a solution containing 1 g/ml) tid for 10-14 days before surgery. Child: As potassium iodide: 50-250 mg (approx 1-5 drops of a solution containing 1 g/ml) tid for 10-14 days before surgery. As strong iodine solution: 0.1-0.3 ml (or approx 3-5 drops) tid. Grave's disease in neonates Child: Neonates: 1 drop of strong iodine solution every 8 hr. Radiation protection against radioactive iodine Adult: As potassium iodide: 100-150 mg 24 hr before procedure and daily for up to 10 days after procedure. Child: As potassium iodide: Infants from birth to 1 mth with a predicted thyroid exposure of =5 centigrays (cGy): 16 mg. >1 mth to 3 yr with a predicted thyroid exposure of =5 cGy: 32 mg. >3 yr to 18 yr (except adolescents approaching adult size) with a predicted thyroid exposure of =5 cGy: 65 mg. Do not exceed once-daily doses. Cutaneous or lymphocutaneous sporotrichosis Adult: As potassium iodide solution containing 1 g/mL: Initially, 1 mL tid, should continue for at least 1 mth after disappearance or stabilisation of the lesions. Child: As potassium iodide: Initially, 250 mg (approx 5 drops of a solution containing 1 g/ml) tid. Max: 1.25-2 g (approx 25-40 drops) tid. Duration: 3-6 mth. Iodine deficiency disorders Adult: As iodised oil (poppyseed/peanut/rapeseed oil containing about 38% w/w or 480 mg/ml of iodine): 400 mg iodine once yrly. Pregnant patient: 200 mg iodine as a single dose. Moderate to severe: 300-480 mg iodine each yr or 100-300 mg iodine every 6 mth and for at least 1 yr postpartum. Child: As iodised oil (poppyseed/peanut/rapeseed oil containing about 38% w/w or 480 mg/ml of iodine): Infants up to 1 yr: Single dose of 100 mg iodine; 1-5 yr: 200 mg iodine; >6 yr: 400 mg iodine. Thyroid storm Adult: As potassium iodide: Up to 500 mg every 4 hr.
Drug Dose no data available
Excess Drug Consumption Symptoms: Metallic taste, vomiting, abdominal pain, bloody diarrhoea, thirst, headache. Systemic toxicity may result in shock, tachycardia, fever, metabolic acidosis, renal impairment. Management: Milk or starch mucilage may be given. Oral treatment may also include activated charcoal or 1% sodium thiosulfate solution.
Forgot Drug Consumption Contact Your doctor
Stop Drug Consumption Do not stop the drug untill your doctor says you to do so.
Possible Side Effects
General Information no data available
Common Drug Side Effects Hypersensitivity reactions (urticaria, angioedema, cutaneous haemorrhage, purpura, fever, arthralgia, lymphadenopathy, eosinophilia); goitre, hypothyroidism and hyperthyroidism. Iodism on prolonged use (metallic taste, increased salivation, swelling and inflammation of throat, swollen and irritated eyes, pulmonary oedema, nausea, vomiting, diarrhoea). Potentially Fatal: Fatal periarteritis, ioderma.
Rare Drug Side Effects no data available
Very Rare Drug Side Effects no data available
Drug Side Effects Symptoms no data available
How to Store the Medicine
How to Store the Medicine Oral solution: Store in tight, light-resistant containers below 40°C (preferably between 15-30°C). Do not freeze. Tablet: Store at 15-30°C.

CALCIUM CARBONATE

Information for patients
Drug Information Calcium carbonate Effervescent Tablets contain Calcium carbonate as the active ingredient (which when dispersed in water provide 500mg of elemental calcium as calcium citrate). The tablets provide extra calcium, in addition to a normal diet, and are used to treat conditions in which the body’s calcium levels need to be increased. Calcium is essential for healthy growth of bones and teeth.
Drug Alert
Alert if you have: • an allergy (hypersensitivity) to any of the ingredients in the product - see Section 6 on “What Calcium carbonate Effervescent Tablets contain”. • an overactive parathyroid gland (hyperparathyroidism) or too much vitamin D in your body (hypervitaminosis D). • a high concentration of calcium in your urine (hypercalciuria) or blood (hypercalcaemia). A high concentration of calcium in the blood may be caused by impaired kidney function, an overactive parathyroid gland, too much Vitamin D in your body or certain bone tumours
Before Consuming the Medicine
Avoid Drug if you have: • an allergy (hypersensitivity) to any of the ingredients in the product - see Section 6 on “What Calcium carbonate Effervescent Tablets contain”. • an overactive parathyroid gland (hyperparathyroidism) or too much vitamin D in your body (hypervitaminosis D). • a high concentration of calcium in your urine (hypercalciuria) or blood (hypercalcaemia). A high concentration of calcium in the blood may be caused by impaired kidney function, an overactive parathyroid gland, too much Vitamin D in your body or certain bone tumours • been immobilised for long periods and had a high concentration of calcium in your blood or urine. • kidney stones
Drug Special Care Consult your doctor before taking this medicine if you have: • a tendency to form kidney stones or impaired kidney function - your treatment will need to be monitored carefully if your kidneys are not working properly to ensure you do not build up too much calcium in your blood. • sarcoidosis (formation of nodules especially in the lymph nodes, lungs, bones and skin
Drug Drug Interactions Please tell your doctor if you are taking or have recently taken any other medicines, including those obtained without a prescription. Seek medical advice before taking Calcium carbonate Effervescent Tablets if you are already taking: • vitamin D • heart medicines such as digoxin and cardiac glycosides • tetracycline antibiotics • thiazide diuretics (water tablets) • bisphosphonates and sodium fluoride (drugs used to treat bone disorders).
Drug Pregnancy Interaction Women who are pregnant or breast-feeding can take Calcium carbonate Effervescent Tablets. Ask your doctor or pharmacist for advice before taking any medicine
Drug Breast feeding Interaction Women who are pregnant or breast-feeding can take Calcium carbonate Effervescent Tablets. Ask your doctor or pharmacist for advice before taking any medicine
Drug Machinery Interaction Calcium carbonate Effervescent Tablets are not expected to affect your ability to drive or operate machinery
Drug More Information Allergy is more common in those people who are allergic to aspirin. Sodium – This medicine contains up to 100mg sodium per dose. To be taken into consideration by patients on a controlled sodium diet.
How to take the Medicine
Consumption Info
Drug quanitty Adults and Elderly: To treat conditions caused by lack of calcium, the dose is usually between 2 and 5 tablets per day. • To prevent bone damage caused by osteoporosis, a dose of 1 to 3 tablets is required per day. • To supplement calcium in your diet, the dose is up to 3 tablets a day. Children: • To treat conditions caused by lack of calcium, the dose is usually between 2 and 5 tablets per day. • To supplement calcium in your diet, the dose is up to 2 tablets a day.
Drug Dose The tablets must be dissolved completely in a glass of water and the solution consumed immediately
Excess Drug Consumption Do not exceed the recommended dose. If you take too much medicine, tell your doctor immediately or visit your nearest Accident & Emergency Department (take the pack with you if possible). Symptoms of overdose may include nausea (feeling sick), polydipsia (excessive thirst), polyuria (frequent passing of urine), constipation
Forgot Drug Consumption If you miss a dose, take the next dose as soon as you remember and continue taking your medicine as before (do not take a double dose). If you have any further questions on the use of this product, ask your pharmacist
Stop Drug Consumption
Possible Side Effects
General Information Like all medicines, Calcium carbonate Effervescent Tablets can cause side effects, although not everybody gets them
Common Drug Side Effects You may suffer an allergic reaction. If you experience rash, itching, difficulty in breathing or swelling of the face, lips, throat or tongue, stop taking the tablets immediately and seek urgent medical help
Rare Drug Side Effects • nausea • abdominal pain • diarrhoea • constipation • wind • skin rashes and itching • high concentration of calcium in the blood (hypercalcaemia) or urine (hypercalciuria)
Very Rare Drug Side Effects
Drug Side Effects Symptoms
How to Store the Medicine
How to Store the Medicine Keep out of the reach and sight of children. Store the product in a dry place. Keep the top of the tube closed with the stopper as Calcium carbonate Effervescent Tablets can be affected by moisture. Do not use Calcium carbonate Effervescent Tablets after the expiry which is stated on the carton after ‘Exp’. The date refers to the last day of that month. Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment.

MANGANESE

Information for patients
Drug Information
Drug Alert
Alert
Before Consuming the Medicine
Avoid Drug
Drug Special Care
Drug Drug Interactions
Drug Pregnancy Interaction
Drug Breast feeding Interaction
Drug Machinery Interaction
Drug More Information
How to take the Medicine
Consumption Info
Drug quanitty
Drug Dose
Excess Drug Consumption
Forgot Drug Consumption
Stop Drug Consumption
Possible Side Effects
General Information
Common Drug Side Effects
Rare Drug Side Effects
Very Rare Drug Side Effects
Drug Side Effects Symptoms
How to Store the Medicine
How to Store the Medicine

ALPHA LIPOIC ACID

Information for patients
Drug Information Alpha-lipoic acid (ALA) has been used as an antioxidant for the treatment of diabetes and HIV. It also has been used for cancer, liver ailments, and various other conditions
Drug Alert
Alert People with diabetes should be careful to check their blood sugar levels because alpha-lipoic acid might lower blood sugar.
Before Consuming the Medicine
Avoid Drug
Drug Special Care
Drug Drug Interactions
Drug Pregnancy Interaction Not enough is known about the use of alpha-lipoic acid during pregnancy and breast-feeding. Stay on the safe side and avoid use.
Drug Breast feeding Interaction
Drug Machinery Interaction
Drug More Information
How to take the Medicine
Consumption Info
Drug quanitty The best dose for neuropathy is 600 mg daily. Between 50 to 100 mg is sufficient for antioxidant purposes. You can buy it in doses of 30 to 100 mg tablets. Studies are mixed about whether or not to take ALA with meals. General antioxidant support: 20 to 50 mg per day Diabetes and diabetic neuropathy: 800 mg per day in divided doses
Drug Dose
Excess Drug Consumption
Forgot Drug Consumption
Stop Drug Consumption
Possible Side Effects
General Information Get emergency medical help if you have signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat. Although not all side effects are known, alpha-lipoic acid is thought to be possibly safe when taken as directed.
Common Drug Side Effects nausea; or skin rash.
Rare Drug Side Effects low blood sugar--headache, hunger, weakness, sweating, confusion, irritability, dizziness, fast heart rate, or feeling jittery; or a light-headed feeling, like you might pass out.
Very Rare Drug Side Effects
Drug Side Effects Symptoms
How to Store the Medicine
How to Store the Medicine Store in cool, dry place. Avoid humidity. In particular , alpha lipoic acid is is stored under 5 degrees

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