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Indiclor

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Overview

What is Indiclor?

INDICLOR Indium In-111 Chloride is a diagnostic radiopharmaceutical intended for radiolabeling ProstaScint (capromab pendetide) used fordiagnostic imaging procedures and for radiolabeling Zevalin (ibritumomab tiuxetan) in preparations used for radioimmunotherapy procedures. It is supplied as a sterile, pyrogen-free solution of Indium (In) Chloride in 0.04M HCl. Each milliliter is supplied at a radioactive concentration of 370 MBq, 10 mCi of Indium In-111 Chloride at time of calibration (no carrier added, with specific activity of > 1.85 GBq/µg Indium, > 50 mCi/µg Indium at time of calibration). The pH of the solution is about 1.4.



What does Indiclor look like?



What are the available doses of Indiclor?

Sorry No records found.

What should I talk to my health care provider before I take Indiclor?

Sorry No records found

How should I use Indiclor?

INDICLOR Indium In-111 Chloride is indicated for radiolabeling of ProstaScint (capromab pendetide) in preparations used fordiagnostic imaging procedures. Indiclor is also indicated for radiolabeling Zevalin (ibritumomab tiuxetan) in preparations used for radioimmunotherapy procedures. Please refer to the package insert for ProstaScint or Zevalin for information regarding the radiolabeled product.

Please refer to the package insert for ProstaScint or Zevalin for this information on the final drug product.


What interacts with Indiclor?

Please refer to the package insert for ProstaScint or Zevalin for this information on the final drug product.



What are the warnings of Indiclor?

Amoxicillin and Clavulanate Potassium 600 mg/42.9 mg per 5 mL should be used with caution in patients with evidence of hepatic dysfunction. Hepatic toxicity associated with the use of amoxicillin/clavulanate potassium is usually reversible. On rare occasions, deaths have been reported (less than 1 death reported per estimated 4 million prescriptions worldwide). These have generally been cases associated with serious underlying diseases or concomitant medications. (See and .)

The contents of the vial of INDICLOR Indium In-111 Chloride solution are intended only to be used as an ingredient for radiolabeling ProstaScint used fordiagnostic imaging procedures and for radiolabeling Zevalin in preparations used for radioimmunotherapy procedures.

Indiclor is not to be administered directly to humans.


What are the precautions of Indiclor?

General

Strict aseptic techniques should be used to maintain sterility throughout the procedures for using this product.

Do not use after the expiration time and date stated on the label.

The contents of the vial are radioactive. Adequate shielding must be maintained at all times.

CARCINOGENESIS, MUTAGENESIS, IMPAIRMENT OF FERTILITY

Please refer to the package insert for ProstaScint or Zevalin for this information on the final drug product.

PREGNANCY CATEGORY

Please refer to the package insert for ProstaScint or Zevalin for this information on the final drug product.

NURSING MOTHERS

Please refer to the package insert for ProstaScint or Zevalin for this information on the final drug product.

PEDIATRIC USE

Please refer to the package insert for ProstaScint or Zevalin for this information on the final drug product.

GERIATRIC USE

Please refer to the package insert for ProstaScint or Zevalin for this information on the final drug product.


What are the side effects of Indiclor?

Please refer to the package insert for ProstaScint or Zevalin for this information on the final drug product.


What should I look out for while using Indiclor?

Please refer to the package insert for ProstaScint or Zevalin for this information on the final drug product.

The contents of the vial of INDICLOR Indium In-111 Chloride solution are intended only to be used as an ingredient for radiolabeling ProstaScint used fordiagnostic imaging procedures and for radiolabeling Zevalin in preparations used for radioimmunotherapy procedures.

Indiclor is not to be administered directly to humans.


What might happen if I take too much Indiclor?

Sorry No Records found


How should I store and handle Indiclor?

StorageStore Pantoprazole Sodium Delayed-Release Tablets at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) see USP Controlled Room Temperature.StorageStore Pantoprazole Sodium Delayed-Release Tablets at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) see USP Controlled Room Temperature.INDICLOR Indium-111 Chloride is supplied in a 2 mL vial containing 0.5 milliliters, 185 MBq, 5.0 mCi of Indium In-111 at calibration time. This packaging design has been carefully selected to minimize leaching of cationic and anionic impurities into the product during transport and storage.NDC 17156-523-01INDICLOR Indium-111 Chloride is supplied in a 2 mL vial containing 0.5 milliliters, 185 MBq, 5.0 mCi of Indium In-111 at calibration time. This packaging design has been carefully selected to minimize leaching of cationic and anionic impurities into the product during transport and storage.NDC 17156-523-01


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Clinical Information

Chemical Structure

No Image found
Clinical Pharmacology

Please refer to the package insert for ProstaScint or Zevalin for this information on the final drug product.

Non-Clinical Toxicology
Please refer to the package insert for ProstaScint or Zevalin for this information on the final drug product.

The contents of the vial of INDICLOR Indium In-111 Chloride solution are intended only to be used as an ingredient for radiolabeling ProstaScint used fordiagnostic imaging procedures and for radiolabeling Zevalin in preparations used for radioimmunotherapy procedures.

Indiclor is not to be administered directly to humans.

Probenecid decreases the renal tubular secretion of amoxicillin. Concurrent use with Amoxicillin and Clavulanate Potassium 600 mg/42.9 mg per 5 mL may result in increased and prolonged blood levels of amoxicillin. Co-administration of probenecid cannot be recommended.

Abnormal prolongation of prothrombin time (increased international normalized ratio [INR]) has been reported rarely in patients receiving amoxicillin and oral anticoagulants. Appropriate monitoring should be undertaken when anticoagulants are prescribed concurrently. Adjustments in the dose of oral anticoagulants may be necessary to maintain the desired level of anticoagulation.

The concurrent administration of allopurinol and ampicillin increases substantially the incidence of rashes in patients receiving both drugs as compared to patients receiving ampicillin alone. It is not known whether this potentiation of ampicillin rashes is due to allopurinol or the hyperuricemia present in these patients. There are no data with Amoxicillin and Clavulanate Potassium 600 mg/42.9 mg per 5 mL and allopurinol administered concurrently.

In common with other broad-spectrum antibiotics, amoxicillin/clavulanate may reduce the efficacy of oral contraceptives.

Strict aseptic techniques should be used to maintain sterility throughout the procedures for using this product.

Do not use after the expiration time and date stated on the label.

The contents of the vial are radioactive. Adequate shielding must be maintained at all times.

Please refer to the package insert for ProstaScint or Zevalin for this information on the final drug product.

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Reference

This information is obtained from the National Institute of Health's Standard Packaging Label drug database.
"https://dailymed.nlm.nih.gov/dailymed/"

While we update our database periodically, we cannot guarantee it is always updated to the latest version.

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Professional

Clonazepam Description Each single-scored tablet, for oral administration, contains 0.5 mg, 1 mg, or 2 mg Clonazepam, USP, a benzodiazepine. Each tablet also contains corn starch, lactose monohydrate, magnesium stearate, microcrystalline cellulose, and povidone. Clonazepam tablets USP 0.5 mg contain Yellow D&C No. 10 Aluminum Lake. Clonazepam tablets USP 1 mg contain Yellow D&C No. 10 Aluminum Lake, as well as FD&C Blue No. 1 Aluminum Lake. Chemically, Clonazepam, USP is 5-(o-chlorophenyl)-1,3-dihydro-7-nitro-2H-1,4-benzodiazepin-2-one. It is a light yellow crystalline powder. It has the following structural formula: C15H10ClN3O3 M.W. 315.72
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Interactions

Interactions

A total of 440 drugs (1549 brand and generic names) are known to interact with Imbruvica (ibrutinib). 228 major drug interactions (854 brand and generic names) 210 moderate drug interactions (691 brand and generic names) 2 minor drug interactions (4 brand and generic names) Show all medications in the database that may interact with Imbruvica (ibrutinib).