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Zinc Acetate Dihydrate 16.8 mg/mL Oral Syrup is a concentrated liquid formulation designed for oral administration. It contains active ingredients and sweeteners, providing a palatable and easy-to-administer dosage form. This syrup is particularly beneficial for pediatric patients or individuals who have difficulty swallowing tablets or capsules. It is commonly used to treat Wilson's disease, a genetic disorder that causes excessive copper accumulation in the body, and to manage zinc deficiency, ensuring adequate zinc levels for optimal health.
Licensed to fill prescriptions for patients in RI, MA, CT, NJ, NH, FL, ME and PA. New York patients are served on a limited basis while nonresident registration is pending.
Zinc Acetate Dihydrate 16.8 mg/mL Oral Syrup is a concentrated liquid medication designed for easy oral administration. This formulation provides a palatable and convenient dosage form, especially suitable for pediatric patients or individuals who have difficulty swallowing tablets or capsules. The syrup contains active zinc acetate dihydrate along with sweeteners to enhance taste and improve compliance.
Zinc acetate dihydrate is primarily used in the management of Wilson's disease, a rare genetic disorder that causes excessive accumulation of copper in the body, leading to liver and neurological problems. Zinc acetate works by inhibiting the absorption of copper from the gastrointestinal tract. It stimulates the production of metallothionein, a protein that binds copper within intestinal cells, preventing its entry into the bloodstream and promoting its elimination through feces.
This medication may also be prescribed for patients with zinc deficiency or in conditions where increased zinc intake is necessary. Adequate zinc levels are essential for numerous bodily functions, including immune system support, wound healing, and DNA synthesis. The oral syrup formulation allows for precise dosing adjustments based on individual patient needs.
Patients should take Zinc Acetate Dihydrate 16.8 mg/mL Oral Syrup exactly as prescribed by their healthcare provider. It is important to follow dosing instructions carefully and not to alter the dose without consulting a medical professional. The syrup should be measured accurately using a calibrated dosing syringe or measuring cup to ensure the correct dose is administered.
Potential side effects may include gastrointestinal discomfort such as nausea, vomiting, stomach pain, or
Zinc Acetate Dihydrate 16.8 mg/mL Oral Syrup is a formulation designed to provide zinc supplementation in a palatable liquid form, which is particularly beneficial for pediatric patients or those who have difficulty swallowing tablets or capsules. Zinc is an essential trace element that plays a crucial role in various biological functions, including immune response, DNA synthesis, and cellular metabolism. This formulation is often used to treat or prevent zinc deficiency, which can occur in various disease states such as acrodermatitis enteropathica, chronic diarrhea, and certain malabsorption syndromes.
When considering the use of Zinc Acetate Dihydrate Oral Syrup, it is important to be aware of potential drug interactions that may affect the efficacy and safety of the treatment. Zinc can interact with a variety of medications, potentially altering their absorption or effectiveness. One of the most notable interactions is with tetracycline and quinolone antibiotics, such as doxycycline, ciprofloxacin, and levofloxacin. Zinc can bind to these antibiotics in the gastrointestinal tract, reducing their absorption and, consequently, their therapeutic efficacy. To minimize this interaction, it is recommended to administer zinc supplements at least 2 hours before or 4-6 hours after taking these antibiotics.
Another important interaction to consider is with penicillamine, a chelating agent used in the treatment of Wilson's disease and rheumatoid arthritis. Zinc can reduce the absorption of penicillamine, potentially decreasing its effectiveness. To avoid this interaction, it is advisable to separate the administration of zinc and penicillamine by at least 2 hours.
Additionally, zinc may interact with diuretics, particularly thiazide diuretics such as hydrochlorothiazide. Thiazide diuretics can increase the renal excretion of zinc, potentially leading to zinc deficiency over time. Patients on long-term thiazide therapy may require monitoring of zinc levels and possible supplementation to prevent deficiency.
Furthermore, zinc can interfere with the absorption of iron and copper when taken in high doses. It is important to monitor patients for signs of iron or copper deficiency if they are on prolonged high-dose zinc therapy. To mitigate this interaction, it is recommended to administer zinc and iron or copper supplements at different times of the day.
Patients and prescribers should also be aware that zinc supplementation can affect the absorption of certain nutrients, such as calcium and magnesium. While these interactions are generally not clinically significant, it is still advisable to monitor patients for any potential nutrient imbalances, especially in those with pre-existing conditions that may affect mineral absorption.
As with any medication, it is crucial to consider the individual patient's medical history, current medications, and overall health status when prescribing Zinc Acetate Dihydrate Oral Syrup. If you have any questions or concerns about potential drug interactions or the appropriate use of this formulation, please reach out to us for further guidance and support.
Zinc Acetate Dihydrate 16.8 mg/mL Oral Syrup is a specialized pharmaceutical formulation designed to deliver zinc in a highly bioavailable form. Zinc is an essential trace element that plays a crucial role in numerous biological processes, including immune function, protein synthesis, wound healing, DNA synthesis, and cell division. This formulation is particularly beneficial for patients who require zinc supplementation but have difficulty swallowing tablets or capsules, such as pediatric patients or those with dysphagia.
The mechanism of action of zinc acetate dihydrate involves the dissociation of zinc ions in the gastrointestinal tract, where they are readily absorbed into the bloodstream. Once absorbed, zinc ions participate in various enzymatic reactions and contribute to the stabilization of cell membranes and the modulation of immune responses. This is particularly important in conditions where zinc deficiency is prevalent or where enhanced zinc intake is necessary to support the body's physiological functions.
In the context of disease states, zinc acetate dihydrate oral syrup can be used to address zinc deficiency, which may manifest in symptoms such as impaired immune function, hair loss, diarrhea, delayed wound healing, and taste abnormalities. It is also utilized in the management of Wilson's disease, a genetic disorder characterized by excessive copper accumulation in the body. In this condition, zinc acts by inducing the production of metallothionein, a protein that binds copper in the intestinal cells, thereby reducing its absorption and promoting its excretion.
The syrup formulation is designed to be palatable and easy to administer, making it an ideal choice for patients who may be averse to or unable to take solid dosage forms. The inclusion of sweeteners and flavoring agents enhances the taste, ensuring better compliance, especially in children. The liquid form also allows for flexible dosing, which can be easily adjusted based on the specific needs of the patient, as determined by their healthcare provider.
For prescribers, it is important to consider the patient's overall nutritional status, potential drug interactions, and specific health conditions when recommending zinc acetate dihydrate oral syrup. Monitoring zinc levels and adjusting the dosage accordingly can help optimize therapeutic outcomes and minimize the risk of adverse effects, such as gastrointestinal discomfort or interference with the absorption of other essential minerals like copper and iron.
If you have any questions or require further information about Zinc Acetate Dihydrate 16.8 mg/mL Oral Syrup, please do not hesitate to reach out to us at Bayview Pharmacy. Our team of compounding pharmacists is here to assist you with any inquiries or concerns you may have regarding this formulation.
Zinc Acetate Dihydrate 16.8 mg/mL Oral Syrup is used to provide zinc supplementation, which is essential for various bodily functions, including immune system support, wound healing, and DNA synthesis. It is often prescribed for individuals with zinc deficiency or specific medical conditions requiring zinc supplementation.
This syrup should be taken orally, as directed by your healthcare provider. It is important to measure the dose accurately using a proper measuring device or spoon. Follow the instructions on the prescription label or as advised by your doctor.
Yes, this formulation is designed to be palatable and easy to administer, making it suitable for pediatric patients who may have difficulty swallowing tablets or capsules. However, always consult a healthcare provider before giving it to children.
Some individuals may experience side effects such as nausea, upset stomach, or a metallic taste in the mouth. If you experience any severe side effects or allergic reactions, seek medical attention immediately.
It is important to inform your healthcare provider about all the medications you are currently taking, as zinc can interact with certain drugs, such as antibiotics and diuretics. Your doctor will advise you on how to manage these interactions.
Store the syrup at room temperature, away from direct sunlight and moisture. Keep it out of reach of children and pets. Do not freeze the syrup, and ensure the bottle is tightly closed when not in use.
If you miss a dose, take it as soon as you remember. If it is almost time for your next dose, skip the missed dose and continue with your regular dosing schedule. Do not double the dose to catch up.
If you are pregnant or breastfeeding, consult your healthcare provider before taking this syrup. They will assess the benefits and potential risks to determine if it is appropriate for your situation.
Your healthcare provider will determine the appropriate duration of supplementation based on your specific needs and medical condition. Long-term use should be monitored by a healthcare professional to avoid potential zinc toxicity.
In case of an overdose, seek immediate medical attention or contact a poison control center. Symptoms of overdose may include nausea, vomiting, dizziness, and difficulty breathing.
This formulation is compounded by Bayview Pharmacy on a prescriber's order for an individual patient. It is not an FDA-approved drug product, and the FDA has not evaluated it for safety, effectiveness, or manufacturing quality.
A valid prescription is required. Availability depends on Bayview's licensure in your state. This page is general information, not medical advice. Discuss your situation with a licensed healthcare provider.
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Compounded preparations have no NDC, so this formula will not appear in your EHR's drug search. Use your system's compound, non-formulary, or free-text prescription entry and name the preparation exactly as written in step 3. If your EHR forces you to pick a listed drug, pick the closest entry for the active ingredient and put the full formula in the prescription body (the Sig or directions field), not in Notes to Pharmacy.
Compounded preparations have no NDC and will not appear in your drug search. For EPCS to validate, select a drug entry your EHR recognizes as controlled, usually the bulk powder entry for the active ingredient (for example Ketamine (bulk) powder, not a branded product), then put the full formula from step 3 in the prescription body. A free-text entry that does not validate as controlled will be rejected by your EPCS module.
Quantity and directions are starting points for this dose form, not treatment recommendations. Dosing remains the prescriber's responsibility.
Transmit from your EHR. For this non-controlled preparation we also accept fax to (401) 284-4506 and phoned orders at (401) 284-4505. Order forms are on the formulation pages and in the prescriber portal.
Transmit with two-factor authentication through your EPCS-enabled EHR. No order form is offered for this preparation; e-prescribing guides for our controlled preparations are on the formulation pages.
Licensed to dispense in RI, MA, CT, NJ, NH, FL, ME, and PA; New York is served on a limited basis while nonresident registration is pending. Compounded preparations are not FDA-approved. A valid prescription is required. Full guide, including steps by EHR: How to e-prescribe to Bayview. Questions about this formula: call (401) 284-4505.
Take orally
