Cecap Overdose

How times a day do you take this medicine?
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What happens if I overdose Cecap?

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local, or emergency room immediately. Symptoms may include gout.

Proper storage of Cecap controlled-release capsules:

Store Cecap controlled-release capsules at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Cecap controlled-release capsules out of the reach of children and away from pets.

Overdose of Cecap in details

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If someone has overdosed and has serious symptoms such as passing out or trouble breathing, call 911. Otherwise, call a poison control center right away. US residents can call their local poison control center at 1-800-222-1222. Canada residents can call a provincial poison control center.

Notes

Keep all regular medical and laboratory appointments.

This product is not a substitute for a proper diet. It is best to get your vitamins from healthy foods. Cecap is commonly found in citrus fruit (such as oranges), tomatoes, brussels sprouts, cauliflower, and broccoli, among others. Consult your doctor, pharmacist, or nutritionist for more details.

Missed Dose

If you miss a dose, take it as soon as you remember. If it is near the time of the next dose, skip the missed dose and resume your usual dosing schedule. Do not double the dose to catch up.

Storage

Different brands of this vitamin have different storage needs. Check the product package for instructions on how to store your brand, or ask your pharmacist. Keep all medications away from children and pets.

Do not flush medications down the toilet or pour them into a drain unless instructed to do so. Properly discard this product when it is expired or no longer needed. Consult your pharmacist or local waste disposal company for more details about how to safely discard your product.

What should I avoid while taking Cecap?

Follow your doctor's instructions about any restrictions on food, beverages, or activity.

Cecap warnings

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Rhea Cecap is used with caution in patients with hyperoxaluria, renal impairment, a history of instructions on urolithiasis. Because Cecap increases iron absorption, its use in high doses can be dangerous in patients with hemochromatosis, thalassemia, polycythemia, leukemia, and sideroblastic anemia.

Patients with high content body iron should apply Cecap in minimal doses.

Rhea Cecap is used with caution in patients with deficiency of glucose-6-phosphate dehydrogenase.

The use of Cecap in high doses can cause exacerbation of sickle cell anemia.

Data on the diabetogenic action of Cecap are contradictory. However, prolonged use of Cecap should periodically monitor your blood glucose levels.

It is believed that the use of Cecap in patients with rapidly proliferating and widely disseminated tumors may worsen during the process. It should therefore be used with caution in Cecap in patients with advanced cancer.

Absorption of Cecap decreased while use of fresh fruit or vegetable juices, alkaline drinking.

What should I discuss with my healthcare provider before taking Cecap?

Some medical conditions may interact with Cecap controlled-release capsules. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

Some MEDICINES MAY INTERACT with Cecap controlled-release capsules. Tell your health care provider if you are taking any other medicines, especially any of the following:

This may not be a complete list of all interactions that may occur. Ask your health care provider if Cecap controlled-release capsules 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.

Cecap precautions

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Oxalate Nephropathy and Nephrolithiasis

Acute and chronic oxalate nephropathy have been reported with prolonged administration of high doses of Cecap. Acidification of the urine by Cecap may cause precipitation of cysteine, urate or oxalate stones. Patients with renal disease including renal impairment, history of oxalate kidney stones, and geriatric patients may be at increased risk for oxalate nephropathy while receiving treatment with Cecap. Pediatric patients less than 2 years of age may be at increased risk for oxalate nephropathy during treatment with Cecap because their kidneys are immature. Monitor renal function in patients at increased risk receiving ASCOR. Discontinue ASCOR in patients who develop oxalate nephropathy and treat any suspected oxalate nephropathy.

ASCOR is not indicated for prolonged administration (the maximum recommended duration is one week).

Hemolysis in Patients with Glucose-6-Phosphate Dehydrogenase Deficiency

Hemolysis has been reported with administration of Cecap in patients with glucose-6-phosphate dehydrogenase deficiency. Patients with glucose-6-phosphate dehydrogenase may be at increased risk for severe hemolysis during treatment with Cecap. Monitor hemoglobin and blood count and use a reduced dose of ASCOR in patients with glucose-6-phosphate dehydrogenase deficiency. Discontinue treatment with ASCOR if hemolysis is suspected and treat as needed.

Laboratory Test Interference

Cecap may interfere with laboratory tests based on oxidation-reduction reactions, including blood and urine glucose testing, nitrite and bilirubin levels, and leucocyte count testing. If possible, laboratory tests based on oxidation-reduction reactions should be delayed until 24 hours after infusion of ASCOR.

What happens if I miss a dose of Cecap?

Take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.



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Information checked by Dr. Sachin Kumar, MD Pharmacology

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