NeuroBloc 10000 IU

90,00 €

NeuroBloc® 10,000 IU is a prescription injectable medication containing botulinum toxin type B, a neurotoxin used to temporarily reduce excessive muscle contractions. It is primarily indicated for the treatment of cervical dystonia (spasmodic torticollis) in adults and should only be administered by healthcare professionals experienced in the use of botulinum toxin products.

NeuroBloc 10,000 IU – Product Description

Product Overview

NeuroBloc 10,000 IU is a medicinal product associate with botulinum toxin type B, a neurotoxin use in specialist medical care for certain neuromuscular conditions. It works by temporarily blocking the release of acetylcholine, a chemical messenger that enables nerves to communicate with muscles. This action can reduce excessive muscle contractions in appropriately select patients.

NeuroBloc is primarily use for the treatment of cervical dystonia, also known as spasmodic torticollis, in eligible patients according to the approve prescribing information. This neurological condition can cause involuntary neck muscle contractions, abnormal head positioning, and discomfort. Treatment decisions should always be made by a qualified healthcare professional after an appropriate clinical assessment.

Key Features of NeuroBloc 10,000 IU

NeuroBloc contains botulinum toxin type B. The state 10,000 IU product designation should be verified against the official packaging, as presentations and labelling may vary by market. It is intend for use by healthcare professionals experience in diagnosing and treating relevant neuromuscular disorders.

By reducing nerve signalling to target muscles, botulinum toxin type B may help manage abnormal muscle activity and associate symptoms. The extent and duration of the response vary between individuals and depend on factors such as the patient’s condition, treatment history, and prescribed regimen.

NeuroBloc is not interchangeable unit-for-unit with other botulinum toxin products. Different formulations have distinct potency units, dosing recommendations, and prescribing instructions. Only the exact prescribed product should be used.

Administration and Storage

NeuroBloc must be administered by an appropriately trained healthcare professional following the manufacturer’s instructions. Before administration, the clinician should verify the product name, concentration, total quantity, expiry date, packaging integrity, and storage history.

Storage and handling requirements must follow the current official product information. Do not use the medicine if the packaging is damaged, the expiry date has passed, or product authenticity and storage conditions cannot be confirmed.

Important Safety Information

Possible side effects include dry mouth, difficulty swallowing, indigestion, and injection-site discomfort. Botulinum toxin products can sometimes cause serious complications, including swallowing or breathing difficulties due to effects beyond the injection site. Patients should seek urgent medical attention if severe or worsening symptoms occur.

Why NeuroBloc Matters in Specialist Care

NeuroBloc provides a specialist treatment option for certain patients with cervical dystonia when prescribed and administered under appropriate medical supervision. Accurate product identification, careful dosing, and ongoing monitoring are essential.

Brand

NeuroBloc

Package Content

1 vial x 10,000 units per pack

Import

This product is from the European Community (EC)

CE-mark

This product is regulated as a medicinal product and does not carry a CE-mark

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