IPRADOL INJECTION 5 µg/2 mL - DISCONTINUED

Country: South Africa

Language: English

Source: South African Health Products Regulatory Authority (SAHPRA)

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                                INDICATIONS [/za_1342.html#1]
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CONTRA-INDICATIONS [/za_1342.html#1]
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IDENTIFICATION [/za_1342.html#1]
  [/za_1342.html#1]    PATIENT INFORMATION
IPRADOL INJECTION 5 ΜG/2 ML - DISCONTINUED
SCHEDULING STATUS:
IPRADOL INJECTION 5 µg/2 mL        S4
PROPRIETARY NAME
(and dosage form):
IPRADOL INJECTION 5 ΜG/2 ML - DISCONTINUED
COMPOSITION:
Each ampoule of 2 mL contains 5 micrograms 
HEXOPRENALINE 
sulphate.
PHARMACOLOGICAL CLASSIFICATION
A 10.2 Bronchodilators.
PHARMACOLOGICAL ACTION
IPRADOL exhibits a long acting bronchospasmolytic effect. In therapeutic doses, heart rate and blood pressure are
only slightly affected.
IPRADOL eliminates functional bronchostenosis by the relaxation of bronchial spasm and in long term treatment
IPRADOL causes a decrease of pathological hypersecretory changes of the bronchial mucosa. IPRADOL provokes an
improved ventilation of the alveoli, a decrease of obstructive reversible pulmonary emphysema and thus a decrease of
respiratory action, which finally normalises the respiratory gas values and the blood count.
INDICATIONS
IPRADOL is a stimulant of the beta receptors in the bronchi and thus a bronchodilator. IPRADOL is effective for the
relief of bronchospasm caused by allergic asthma, acute, sub-acute and chronic bronchitis and emphysema. 
CONTRA-INDICATIONS
Hypersensitivity to any of the ingredients.
Safety in pregnancy and lactation has not been established. IPRADOL should be used with great care in patients with
cardiovascular disease such as ischeamic heart disease, arrhythmia or tachycardia, occlusive v
                                
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