Netspot

Medical Author: John P. Cunha, DO, FACOEP Last updated on RxList: 1/6/2022
Netspot Side Effects Center

Medical Editor: John P. Cunha, DO, FACOEP

What Is Netspot?

Netspot (kit for the preparation of gallium Ga 68 dotatate injection), after radiolabeling with Ga 68, is a radioactive diagnostic agent indicated for use with positron emission tomography (PET) for localization of somatostatin receptor positive neuroendocrine tumors (NETs) in adult and pediatric patients.

What Are Side Effects of Netspot?

Side effects of Netspot are not expected. Tell your doctor if you experience any side effects while Netspot is administered.

Dosage for Netspot

Netspot is supplied as a single dose kit containing: Vial 1 (reaction vial with lyophilized powder) containing 40 mcg of dotatate, and Vial 2 (buffer vial) containing 1 mL of reaction buffer solution.

What Drugs, Substances, or Supplements Interact with Netspot?

Netspot may interact with non-radioactive somatostatin analogs. Tell your doctor all medications and supplements you use.

Netspot During Pregnancy or Breastfeeding

Netspot is not recommended for use during pregnancy. All radiopharmaceuticals, Netspot, have the potential to cause fetal harm. Netspot is not recommended for use while breastfeeding. Breast milk should be pumped and discarded for 12 hours after administration of Netspot.

Additional Information

Our Netspot (kit for the preparation of gallium Ga 68 dotatate injection) Side Effects Drug Center provides a comprehensive view of available drug information on the potential side effects when taking this medication.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

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Netspot Professional Information

SIDE EFFECTS

The following clinically significant adverse reactions are described elsewhere in the labeling:

  • Hypersensitivity reactions [see WARNINGS AND PRECAUTIONS]

Clinical Trials Experience

The safety of Ga 68 dotatate was evaluated in three single center studies [see Clinical Studies] and in a survey of the scientific literature. No serious adverse reactions were identified.

Postmarketing Experience

The following adverse reactions have been identified during post-approval use of NETSPOT or other somatostatin receptor imaging agents. 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 the drug.

Gastrointestinal Disorders: Nausea and vomiting

General Disorders and Administration Site Conditions: Injection site pain and burning sensation

Immune System Disorders: Hypersensitivity reactions, predominantly rash, pruritus, less frequently angioedema or features of anaphylaxis.

DRUG INTERACTIONS

Non-radioactive somatostatin analogs competitively bind to the same somatostatin receptors as Ga 68 dotatate. Image patients with Ga 68 dotatate PET just prior to dosing with long-acting analogs of somatostatin. Shortacting analogs of somatostatin can be used up to 24 hours before imaging with Ga 68 dotatate.

Corticosteroids can down-regulate somatostatin subtype 2 receptors. Repeated administration of high doses of glucocorticoid prior to Ga 68 dotatate administration may result in false negative imaging.

Read the entire FDA prescribing information for Netspot (Gallium Ga 68 Dotatate Kit)

SLIDESHOW

Digestive Disorders: Common Misconceptions See Slideshow

© Netspot Patient Information is supplied by Cerner Multum, Inc. and Netspot Consumer information is supplied by First Databank, Inc., used under license and subject to their respective copyrights.

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