CEREBRUM COMPOSITUM NM

CEREBRUM COMPOSITUM NM ampoules

Important notes (mandatory information)

Cerebrum compositum NM, liquid dilution for injection. Areas of application: Registered homeopathic medicinal product, therefore without indication of a therapeutic indication.

For risks and side effects, read the package leaflet and ask your doctor or pharmacist.


PACKAGE LEAFLET: INFORMATION FOR THE USER

Cerebrum compositum NM, liquid dilution for injection

Homeopathic medicinal product.
Registered homeopathic medicinal product, therefore without indication of a therapeutic indication. If symptoms persist, seek medical advice.

Contraindications

Do not use in case of hypersensitivity to quinine.

Precautions for use

Like all medicines, homeopathic medicines should only be used during pregnancy and breastfeeding after consulting a doctor. There is insufficient documented experience with the use of this medicine in children. It should therefore not be used in children under 12 years of age.

Interactions

None known. General note: The effect of a homeopathic medicinal product can be adversely affected by generally harmful factors in the lifestyle and by stimulants and luxury foods. If you are taking other medicines, ask your doctor.

Type of application

The application requires individual dosage by a homeopathically experienced therapist.

Duration of treatment

Even homeopathic medicines should not be used for a long period of time without medical advice.

Side effects

In individual cases, skin reactions may occur; the product should then be discontinued. In persons with known hypersensitivity to Compositae (Arnica), hypersensitivity reactions (up to anaphylactic reaction) are possible in individual cases. Redness, swelling and pain at the injection site may occur temporarily. In rare cases, hypersensitivity reactions such as skin allergies or fever may occur after the use of quinine-containing medicines. In these cases, a doctor should be consulted. Note: Sensitisation to quinine or quinidine is possible.
Note: When using homeopathic medicines, existing symptoms may temporarily worsen (initial aggravation). In this case, you should stop taking the medicine and consult your doctor. If you notice any side effects, please contact your doctor or pharmacist. This also applies to side effects not listed in this package leaflet. You can also report side effects directly to the Federal Institute for Drugs and Medical Devices, Department of Pharmacovigilance, Kurt-Georg-Kiesinger-Allee 3, D-53175 Bonn, website: www.bfarm.de. By reporting side effects, you can help provide more information about the safety of this medicine.

Notes on expiry date and storage

Keep medicine out of reach of children! The expiry date of this pack is printed on the container and outer packaging. Do not use this pack after this date. No special storage conditions are required for this medicine.

Composition

1 ampoule of 2.2 ml (= 2.2 g) contains: Active ingredients: Cerebrum suis Dil. D8 (HAB, prescription 42a) 22 mg, Embryo suis Dil. D10 (HAB, prescription 42a) 22 mg, Hepar suis Dil. D10 (HAB, prescription 42a) 22 mg, Placenta suis Dil. D10 (HAB, prescription 42a) 22 mg, Kalium phosphoricum Dil. D6 22 mg, Selenium Dil. D10 22 mg, Thuja occidentalis Dil. D6 22 mg, Strychnos ignatii Dil. D8 22 mg, Acidum phosphoricum Dil. D10 22 mg, Cinchona pubescens Dil. D4 22 mg, Sulfur Dil. D10 22 mg, Kalium bichromicum Dil. D8 22 mg, Gelsemium sempervirens Dil. D4 22 mg, Ruta graveolens Dil. D4 22 mg, Arnica montana Dil. D28 22 mg, Aesculus hippocastanum Dil. D4 22 mg, Manganum phosphoricum Dil. D8 aquos. (HAB, prescription 6) 22 mg, Magnesium phosphoricum Dil. D10 22 mg, Semecarpus anacardium Dil. D6 22 mg, Conium maculatum Dil. D4 22 mg, Hyoscyamus niger Dil. D6 22 mg, Aconitum napellus Dil. D6 22 mg, Anamirta cocculus Dil. D4 22 mg, Ambra grisea Dil. D10 22 mg. Active ingredients 1 to 16 and 18 to 24 are potentised together over the last 2 stages. Other ingredients: Water for injections, sodium chloride.

Pack sizes

Liquid dilution for injection. 10 ampoules; hospital pack with 50 and 100 ampoules of 2.2 ml each.

Pharmaceutical entrepreneur and manufacturer

Biologische Heilmittel Heel GmbH
Dr.-Reckeweg-Str. 2-4
76532 Baden-Baden
Telephone: 07221 501-00
Fax: 07221 501-210
E-mail: info@heel.de

This package leaflet was last revised in September 2014.

Source: Package leaflet information
Status: 01/2016
Areas of application: Registered homeopathic medicinal product, therefore without indication of a therapeutic indication.