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EMA Product

GoResp Digihaler (previously Budesonide/Formoterol Teva Pharma B.V.)

Product approved by European Medicines Agency (EU)

Basic Information

GoResp Digihaler (previously Budesonide/Formoterol Teva Pharma B.V.)

Regulatory Information

EMEA/H/C/004882

Authorised

April 3, 2020

January 30, 2020

6

February 18, 2025

Company Information

the netherlands

Teva Pharma B.V. Swensweg 5 2031GA Haarlem

Teva Pharma B.V.

Active Substances Detail

Budesonideformoterol fumarate dihydrate

Detailed Information

Therapeutic Indication

### Therapeutic indication Budesonide/Formoterol Teva Pharma B.V. is indicated in adults 18 years of age and older only. Asthma Budesonide/Formoterol Teva Pharma B.V. is indicated in the regular treatment of asthma, where use of a combination (inhaled corticosteroid and long-acting β2 adrenoceptor agonist) is appropriate: -in patients not adequately controlled with inhaled corticosteroids and “as needed” inhaled short-acting β2 adrenoceptor agonists. or -in patients already adequately controlled on both inhaled corticosteroids and long-acting β2 adrenoceptor agonists. COPD Symptomatic treatment of patients with COPD with forced expiratory volume in 1 second (FEV1) < 70% predicted normal (post bronchodilator) and a history of repeated exacerbations, who have significant symptoms despite regular therapy with long-acting bronchodilators.

Overview Summary

Budesonide/Formoterol Teva Pharma B.V. is a medicine used for the treatment of asthma in adults for whom a combination product is considered appropriate. It can be used in patients: - whose disease is not adequately controlled by treatment with other asthma medicines called corticosteroids and ‘short-acting beta-2 agonists’ taken by inhalation; - whose disease is adequately controlled by treatment with corticosteroids and ‘long-acting beta-2 agonists’ taken by inhalation. Budesonide/Formoterol Teva Pharma B.V. is also used to relieve the symptoms of severe chronic obstructive pulmonary disease (COPD) in adults who have had exacerbations (flare–ups) of the disease in the past despite regular treatment. COPD is a long-term disease in which the airways and air sacs inside the lungs become damaged or blocked, leading to difficulty in breathing. Budesonide/Formoterol Teva Pharma B.V. is a ‘hybrid medicine’. This means that it is similar to a ‘reference medicine’ containing the same active substances, but Budesonide/Formoterol Teva Pharma B.V. is given using a different inhaler. The reference medicine for Budesonide/Formoterol Teva Pharma B.V. is Symbicort Turbohaler. Budesonide/Formoterol Teva Pharma B.V. contains the active substances budesonide and formoterol.

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