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Content Reviewed By:
Dr. Manoj Shah
, (MBBS)
Written By:
Ms. Priyanka Shah
, (B.Pharm)
While SHARKOFERROL TONIC 450 GM is generally safe, some individuals may experience side effects. These can include gastrointestinal issues like nausea, vomiting, diarrhea, or constipation. Some individuals might also experience abdominal pain or stomach upset. Allergic reactions, though rare, can occur, manifesting as skin rashes, itching, or swelling. In very rare cases, severe allergic reactions (anaphylaxis) are possible. High doses may lead to iron overload, causing symptoms like fatigue, joint pain, and organ damage. It is important to adhere to the recommended dosage. Consult your doctor if any side effects persist or worsen.

Overdose and misuse
Medical emergency in overdoseAccidental or intentional overdose of iron‑containing products such as Sharkoferrol can be dangerous, particularly in young children, and may lead to serious toxicity including vomiting, diarrhea, abdominal pain, metabolic acidosis, shock, and organ failure.
Sharkoferrol Tonic 450 GM is typically used as a health supplement, providing a source of vitamins, minerals, and other nutrients. It aims to improve overall health and well-being.
The main ingredients of Sharkoferrol Tonic 450 GM typically include shark liver oil, iron, calcium, vitamin D, and other vitamins and minerals. The exact composition may vary depending on the brand.
Side effects of Sharkoferrol Tonic 450 GM are rare, but may include nausea, stomach upset, or allergic reactions. Discontinue use and consult a doctor if you experience any side effects.
Store Sharkoferrol Tonic 450 GM at room temperature, away from direct sunlight and moisture. Keep out of reach of children.
Pregnant women should consult their doctor before using Sharkoferrol Tonic 450 GM.
Refer to the product label or consult your doctor for the recommended dosage of Sharkoferrol Tonic 450 GM.
Consult a pediatrician before giving Sharkoferrol Tonic 450 GM to children.
Sharkoferrol Tonic 450 GM can be taken with or without food, but it is recommended to take it with food for better absorption.
If you miss a dose of Sharkoferrol Tonic 450 GM, take it as soon as you remember. If it is close to your next dose, skip the missed dose and continue with your regular dosing schedule.
Consult your doctor before taking Sharkoferrol Tonic 450 GM with other medications, as it may interact with some drugs.
Sharkoferrol Tonic 450 GM contains shark liver oil, which makes it unsuitable for vegetarians.
Sharkoferrol Tonic 450 GM is used to address deficiencies in vitamins, minerals, and iron.
Sharkoferrol Tonic 450 GM can help boost energy levels by reducing feelings of fatigue and weakness.
Symptoms of an overdose with Sharkoferrol Tonic 450 GM may include nausea, vomiting, stomach pain, and diarrhea. Seek immediate medical attention if you suspect an overdose.
The vitamins and minerals present in Sharkoferrol Tonic 450 GM can help in boosting the immune system.
Sharkoferrol is a multinutrient tonic that typically contains iron (such as ferric ammonium citrate), calcium, vitamin D3, vitamin B12, niacinamide, and folic acid. It is generally used as a nutritional supplement in individuals with increased requirements or documented deficiencies of these nutrients, for example in nutritional anemia, poor dietary intake, convalescence, or certain chronic conditions, as assessed by a healthcare professional.
Sharkoferrol functions as both an iron supplement and a general multinutrient tonic. Iron is one of its key components, but it also provides calcium, vitamin D3, B‑complex vitamins, and folic acid. Because of this combination, it is used not only to support iron status but also to help maintain bone health and overall micronutrient balance when clinically indicated.
In some regions Sharkoferrol or similar tonics may be available without a prescription, but self‑medication is not advisable. Iron, calcium, and vitamin D3 can cause harm if taken inappropriately or in excess, and they may interact with other medicines. A healthcare professional should first evaluate your symptoms, diet, and laboratory results to determine whether Sharkoferrol is suitable and necessary for you.
Commonly reported adverse effects are related mainly to the iron and calcium components and may include nausea, abdominal discomfort, constipation, diarrhea, metallic taste, and darkening of stools. Some individuals may experience mild bloating or gas. B‑complex vitamins are usually well tolerated, but niacinamide can occasionally cause flushing or gastrointestinal upset. Any persistent or severe symptoms should be discussed with a healthcare professional.
Iron, folic acid, vitamin B12, calcium, and vitamin D3 are all important in pregnancy, but the exact amounts required vary and should be tailored to the individual. Sharkoferrol should only be used during pregnancy on the advice of a qualified healthcare professional who can assess your dietary intake, blood tests, and any other supplements or medications you are taking, and then decide whether this specific product and dose are appropriate.
The nutrients present in Sharkoferrol, such as iron, calcium, vitamin D3, folic acid, and vitamin B12, are generally compatible with breastfeeding when used at recommended therapeutic doses. However, the total intake from diet, other supplements, and any prescribed medications must be considered. A healthcare professional should confirm whether Sharkoferrol is necessary and safe for you during lactation and advise on duration of use.
Use in children depends on age, body weight, nutritional status, and the specific formulation and concentration of Sharkoferrol available in your region. Pediatric dosing of iron, calcium, and vitamins must be carefully adjusted to avoid under‑ or overdosing. Therefore, Sharkoferrol should not be given to children without direct guidance from a pediatrician or qualified healthcare professional who can select the correct product and regimen.
Sharkoferrol should generally be avoided or used only under specialist supervision in individuals with known hypersensitivity to any of its components, hereditary disorders of iron overload such as hemochromatosis or hemosiderosis, severe liver disease with iron accumulation, severe renal impairment or a history of recurrent kidney stones, hypercalcemia, or conditions associated with vitamin D hypersensitivity. Patients already receiving high‑dose iron, calcium, vitamin D, or B‑complex therapy should also be evaluated carefully before adding Sharkoferrol.
Yes. Iron and calcium can reduce the absorption of several oral medicines, including certain antibiotics (such as some tetracyclines and fluoroquinolones), levothyroxine, and some bisphosphonates, if taken at the same time. Conversely, some drugs, such as proton pump inhibitors or antacids, may reduce iron absorption. High doses of folic acid can influence the effect of some anticonvulsants. Because of these potential interactions, you should provide your healthcare professional with a complete list of all medicines and supplements you use before starting Sharkoferrol.
The duration of use should be individualized and based on the underlying indication, laboratory monitoring, and clinical response. In many cases, iron‑containing supplements are used for a defined course until iron stores and hemoglobin normalize, followed by reassessment. Long‑term, unsupervised use is not recommended because chronic excess intake of iron, calcium, or vitamin D3 can lead to toxicity or organ damage. Your prescriber should determine the appropriate treatment duration and follow‑up schedule.
If you miss a dose, take it as soon as you remember, unless it is almost time for your next scheduled dose. In that case, skip the missed dose and resume your regular dosing schedule. Do not double the dose to make up for a missed one, as this may increase the risk of gastrointestinal discomfort or other adverse effects. If you frequently forget doses, discuss adherence strategies with your healthcare professional.
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