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DIALGIN 500 mg. 20 sachets

Brand: ACTAVIS
Product Code: DIALGIN 500 mg. 20 sachets
Availability: In Stock
Product viewed: 3908

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DIALGIN 500 mg. 20 sachets

COMPOSITION
Each sachet Dialgin 500 mg contains as active drug substance 500 mg metamizole sodium and the following inactive ingredients: mannitol, sodium cyclamate and strawberry flavor.
• PHARMACEUTICAL FORM
Sachet of powder for oral use
• Pharmacotherapeutic group
Non-opioid analgesics
• WHAT IT IS USED DIALGIN
1. pains
For the symptomatic treatment of pain from different backgrounds and with different intensity when other agents are contraindicated: headache, migraine, toothache, joint and muscle pain; post-traumatic and post-operative pain, renal and biliary colic; pain in cancer.
2. For life-threatening lowering of high body temperature, when the other agents are ineffective or contra ..


ATTENTION!
• WHEN NOT TO TAKE DIALGIN
This medicine should not be accepted in the following cases: -
• Hypersensitivity to metamizole or any of the excipients;
• Hypersensitivity to products of the same group;
• Severe liver and kidney diseases;
• Hypersensitivity to pyrazolone derivatives;
• Allergic reactions to aspirin or other medicines pronivovazpalitelni, rhinitis, urticaria, asthma;
• Blood dyscrasias;
• Diseases of the hematopoietic system;
• Porphyria;
• Genetic deficiency of glucose-6-phosphate dehydrogenase;
• Pregnancy;
• Children under 14 years of age.
When in doubt ALWAYS ASK YOUR DOCTOR OR PHARMACIST FOR ADVICE.

• SPECIAL WARNINGS AND PRECAUTIONS FOR USE
Dialgin should be administered with caution in the following cases:
1. Gastrointestinal diseases (ulcers, bleeding, perforation)
2. Impaired renal function
3. Hypertension
4. Fluid retention and edema
5. Impaired liver function
6. Serious infectious diseases
7. Simultaneous use of chlorpromazine
8. It is possible when taking the drug appeared red colored urine.
9. To monitor indicators of blood cell counts in cancer patients.
10. During treatment with chlorpromazine be administered after consulting a doctor.
11. In patients with acute renal failure Dialgin dose should be reduced (preferably one sachet per day).


• interactions with other drugs or other forms of interaction
• Plasma levels of cyclosporine were reduced when administered with Dialgin;
• Dialgin can reduce the natriuretic and antihypertensive effects of ACE inhibitors;
• Dialgin may increase the plasma concentrations of lithium and lithium cause toxicity;
• Neuroleptics, tranquilized products potentiate the analgesic effect;
• antidepressants, oral contraceptives, allopurinol - slow metabolism and may increase its toxicity;
• combination with chlorpromazine may increase the risk of severe hypothermia; © Coadministration with coumarin anticoagulants reduces their effectiveness;
• Risk of damage to the WBC in the simultaneous acceptance of the product with medicines that suppress bone marrow function, as products containing gold and anticancer products.

To avoid possible interactions between several medicinal products, always inform your doctor or pharmacist if you are taking other medicines.


• Pregnancy and lactation
Dialgin should not be used during pregnancy and lactation ..


During pregnancy and lactation Always consult your doctor or pharmacist before taking MEDICAL PRODUCT

• DRIVE AND USE MACHINES
No data Dialgin influence on the ability to drive and use machines.

HOW TO TAKE DIALGIN

• Method and route of administration
The contents of the sachet 1 was dissolved in a glass of water and drunk.

• DOSAGE
Adults and children over 14 years of age is recommended by 1 sachet 1-3 times daily. Maximum daily dose is 6 sachets (3 g) .Dialgin should be used for the shortest possible period of time.


SIDE EFFECTS
1. Hypersensitivity - anaphylactic shock;
2. Hematologic - hemolytic anemia, aplastic anemia; agranulocytosis, leukopenia, thrombocytopenia;
3. genitourinary - oliguria, proteinuria, interstitial nephritis;
4. Dermatological - hives, rashes and itching, toxic epidermal necrolysis, pemphigus vulgaris, diaforezis (sweating);
5. Respiratory - bronchospasm;
6. Gastrointestinal - nausea, vomiting;

DO NOT HESITATE TO they ask your doctor or pharmacist for advice INFORM THEM OF ANY unwanted or unpleasant effects you noticed AND IS NOT listed in this leaflet.


STORAGE
• DO NOT USE AFTER THE PREPARATION on the outer package
Shelf life 3 years.

• SPECIAL WARNING STORAGE
Keep at 15 to 25 ° C dry and reach of children.

 

 

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