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Sodium metamizol exerts both an analgesic and antispasmodic action. This spasmolytic action is re-inforced by a papaverine analogue, pitofenone hydrochloride, and a component with parasympatholytic action, fenpiverinium bromide.
Colic of the biliary, urinary and gastro-intestinal tract. Spastic conditions of the female genital system.
BARALGAN???? should not be administered to patients with a known history of sensitivity to pyrazolone derivatives. It is further contra-indicated in patients suffering from hepatic porphyria, congenital glucose-6-phosphate dehydrogenase deficiency, tachyarrythmias, narrow-angle glaucoma, prostatic hypertrophy with a tendency to urine retention, mechanical obstruction of the gastro-intestinal tract, megacolon.
Patients who suffer from bronchial asthma or chronic respiratory infections and patients with a history of other hypersensitivity reactions, also to substances other than medicines, belong to a risk group which, on using any analgesic or antirheumatic, may develop shock (analgesic intolerance). Such predisposition may also exist in patients who react to small amounts of alcoholic beverages with sneezing, running eyes and severe facial flushing.
The risk of shock is comparatively higher after parenteral than after oral administration. Before starting BARALGAN???? treatment the patient should be questioned about a history of hypersensitivity reactions.
DOSAGE AND DIRECTIONS FOR USE:
The stated doses are given three times a day:
Adults and adolescents of 15 years and older: 1 - 2 tablets
Children 7 - 14 years 1/2 - 1 tablet
Tablets should be swallowed whole with some liquid
SIDE-EFFECTS AND SPECIAL PRECAUTIONS
Side-effects may include hypersensitivity reactions of the skin and mucosa of the eyes, nose and throat.
Granulocytopenia progressing to agranulocytosis, and shock may also occur. These are always serious.
The symptoms of agranulocytosis are: high fever, chills, sore-throat, dysphagia, inflammation in the regions of mouth, nose, throat and in the anogenital region. If this condition is suspected, blood counts must be performed and BARALGAN???? treatment discontinued immediately. If the suspicion is confirmed, appropriate countermeasures must be initiated without delay.
The symptoms of shock (more common with parenteral administration) are pruritus, cold sweat, dizziness, stupor, nausea, flushing or pallor of the skin and dyspnoea.
At the first signs of shock, the preparation must be discontinued immediately, the patient must be put into a supine position with legs raised and airways patent and standard emergency measures must be initiated for the treatment of anaphylactic shock.
Other allergic reactions may include that of the skin and the mucosa of the eyes, nose and throat.
If BARALGAN causes any type of hypersensitivity reaction, the patient must be warned against the future use of any pyrazolone-containing preparation.
Anticholinergic side-effects such as dry mouth, tachycardia, disturbances in visual accommodation, micturition difficulties and constipation may occur.
If quinidine is administered concomitantly with BARALGAN potentiation of the anticholinergic effects may occur.
Abstinence from alcohol is recommended during BARALGAN therapy since mutual influence cannot be excluded.
In patients treated with BARALGAN, enzymatic blood sugar determinations using the glucose-oxydase method may yield incorrectly low values.
Safety in pregnancy has not been established. Because of its long duration of action BARALGAN???? should not be used during childbirth and for the dilation of the cervical canal for curettage. In infants and small children, and in patients with pre-existing dyshaematopoiesis or with unstable circulatory conditions e.g. RR systolic &lt; 100 mm/Hg), BARALGAN???? must only be used under medical supervision.
KNOWN SYMPTOMS OF OVERDOSAGE AND PARTICULARS OF ITS TREATMENT:
In the event of accidental poisoning or overdosage treatment of any toxic effects is symptomatic and supportive.
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