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Molecule

Centruroides fab2 antivenin (equine)

Antivenin
Available on requestBiologic
Presentations
1
Brands
1
Manufacturers
1
Available from stock
0

Centruroides fab2 antivenin (equine) is an antivenin indicated for the treatment of clinical signs of scorpion envenomation. It is available as powder for injection for intravenous use. MedsAcross supplies Centruroides fab2 antivenin (equine) for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Key facts

Pharmacological class
Antivenin, Venom Neutralization, Passively Acquired Immunity
US FDA first approval
Not recorded
EU status
Not recorded
Orphan designation
Not recorded
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Intravenous
Dosage forms
Powder for injection
Biologic
Yes
Identifiers
UNII DDA050FCEA

Clinical information

From the regulator-approved product information. Each section names its source.

Uses

ANASCORP is an antivenin indicated for the treatment of clinical signs of scorpion envenomation. ANASCORP® [centruroides (scorpion) immune F(ab') 2 (equine) injection] is an equine-derived antivenom indicated for treatment of patients with clinical signs of scorpion envenomation.

Source: US FDA prescribing information

How it works

ANASCORP is composed of venom-specific F(ab') 2 fragments of immunoglobulin G (IgG) that bind and neutralize venom toxins, facilitating redistribution away from target tissues and elimination from the body. 1

Source: US FDA prescribing information

Dosing overview

Intravenous use only. Initial Dose 3 vials Reconstitute each vial with 5 milliliters of sterile normal saline (0.9% NaCl). Combine and further dilute to a total of 50 milliliters. Infuse intravenously over 10 minutes. Additional dose (s) As needed Administer one vial at a time at 30-60 minute intervals. Dilute to a total of 50 milliliters with sterile normal saline (0.9% NaCl). Initiate treatment with ANASCORP as soon as possible after scorpion sting in patients who develop clinically important signs of scorpion envenomation, including but not limited to loss of muscle control, roving or abnormal eye movements, slurred speech, respiratory distress, excessive salivation, frothing at the mouth, vomiting. Close patient monitoring is necessary. For Intravenous use only.

Source: US FDA prescribing information

Warnings and precautions

Severe hypersensitivity reactions, including anaphylaxis, are possible with ANASCORP. Prepare for monitoring and management of allergic reactions, particularly in patients with a history of hypersensitivity to equine (horse) proteins or patients who have received previous therapy with antivenoms containing scorpion or equine proteins. Delayed allergic reactions (serum sickness) may occur following treatment with ANASCORP. Patient monitoring with follow-up visit is recommended. ANASCORP is made from equine plasma and may contain infectious agents, e.g. viruses. Localized reactions and generalized myalgias have been reported with the use of cresol as an injectable excipient.

Source: US FDA prescribing information

Side effects

The most common adverse reactions observed in ≥ 2% of patients in the clinical studies for ANASCORP were: vomiting, pyrexia, rash, nausea and pruritus.

Source: US FDA prescribing information

Storage

Store at room temperature (up to 25 ºC (77 ºF)). Brief temperature excursions are permitted up to 40 ºC (104ºF). DO NOT FREEZE.

Source: US FDA prescribing information

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

All presentations

1 presentations of Centruroides fab2 antivenin (equine), sorted by availability.

MedicineManufacturerRegisterAvailability
Anascorp 7 mg/mL powder for injectionIntravenousRare Disease TherapeuticsUS FDAAvailable on request

Brands by market

1 brand names across 1 markets.

Brand names by country

United States

Manufacturers

Regulatory status

Approval facts from US FDA, EMA and CDSCO data, and registration status by country where we hold register data.

RegisterStatusSource
US FDANot recorded—
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Questions and answers

Is Centruroides fab2 antivenin (equine) available for export from India?

Yes, on request. MedsAcross lists 1 presentations of Centruroides fab2 antivenin (equine) and sources them for licensed hospitals, importers and physicians against valid import documents.

What brand names does Centruroides fab2 antivenin (equine) have?

The catalogue lists 1 brand names for Centruroides fab2 antivenin (equine), including Anascorp.

Does Centruroides fab2 antivenin (equine) need cold chain shipping?

No listed presentation of Centruroides fab2 antivenin (equine) is recorded as needing a cold chain. Storage conditions are shown on each presentation page.

References

  1. ANASCORP prescribing information (Rare Disease Therapeutics). U.S. National Library of Medicine, DailyMed. Retrieved 16 July 2025

Request Centruroides fab2 antivenin (equine) for export supply

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