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Cardiogen-82

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Cardiogen-82

SIDE EFFECTS

Postmarketing Experience

The following serious adverse reactions have been identified during postapproval use of CardioGen-82. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

Unintended radiation exposure has occurred in some patients who received rubidium Rb 82 chloride injections at clinical sites where generator eluate testing appeared insufficient [see BOXED WARNING, WARNINGS AND PRECAUTIONS, and DOSAGE AND ADMINISTRATION].

Read the Cardiogen-82 (rubidium rb 82 generator) Side Effects Center for a complete guide to possible side effects

DRUG INTERACTIONS

Specific drug-drug interactions have not been studied.

Last reviewed on RxList: 2/15/2012
This monograph has been modified to include the generic and brand name in many instances.

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Report Problems to the Food and Drug Administration

 

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.


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