NIFLURIL 700 mg. 8 suppositories

What your medicine?
Each suppository contains as active ingredient 700 mg acting MorniflumateKato adjuvant drug containing solid fat type Suppocire BM
 
How comes your medicine?
Nifluril 700mg for adults is presented as a suppository.
 
 
What is Nifluril?
NSAID (M: musculoskeletal system)
 
 
What is this medicine?
This drug is indicated for use in adults and children over 12 years of age:
- Symptomatic treatment of rheumatoid arthritis
- And invalidate some painful osteoarthritis;
- Short-term symptomatic treatment of acute arthritic attack.
 
 
How to use this medicine?
DOSAGE
RESTRICTED TO ADULTS AND CHILDREN OVER 12 YEARS.
The usual dose is one suppository twice daily, ie 1400 mg morniflumat 24 hours ..
 
MUST ALWAYS BE STRICTLY OBSERVED your doctor's prescription.
 
 
When you should not apply this medicine?
This medicine should not be used in the following cases:
- The sixth month of pregnancy
- A known allergy to the drug or drug-related, in particular other NSAIDs or aspirin,
- Active gastric ulcer or duodenal ulcer,
- Severe liver disease,
- Severe kidney disease
- Children under 12 years of age
- Hypersensitivity to any of the excipients.
 
This medicine should not be used unless a medical prescription;
• in the case of treatment with:
- Oral anticoagulants
- Other non-steroidal anti-inflammatory agents,
- Aspirin in high doses,
- Heparin for injection,
- Lithium,
- Methotrexate at high doses
- Ticlopidine,
• During the first 5 months of pregnancy,
• breast-feeding
IF YOU HAVE ANY DOUBTS CONSULT YOUR DOCTOR. SPECIAL PREDUPREZHDENIYALECHENIETO this medicine REQUIRED MEDICAL MONITORING.
In case of infection requires close monitoring.
 
 
PRECAUTIONS FOR USE
Due to the need to adjust your treatment, it is important to inform your doctor in case of:
- Indigestion (hiatal hernia, gastrointestinal bleeding, passed a stomach ulcer or duodenal)
- Heart disease, liver or kidney;
- Asthma: in some patients the appearance of asthmatic attacks may be associated with allergies to aspirin or nonsteroidal anti-inflammatory drug. It is contraindicated in such cases.
- As with any drug to inhibit prostaglandin synthesis, this drug can lead to impaired fertility and is not recommended for women planning pregnancy. Termination of its use should be considered in patients with suspected or during diagnostic procedures for infertility.
 
 
Are Possible interactions between Nifluril and other drugs?
TO AVOID POTENTIAL drug interaction, you should always tell your doctor if you take other medicines:
other non-steroidal anti-inflammatory drugs, oral anticoagulants, aspirin at high doses of heparin for injection, lithium, high-dose methotrexate, ticlopidine.
 
Pregnancy and lactation
Your doctor, if necessary, can prescribe this medicine during the first five months of bremennostta.Nezavisimo circumstances, this medication should not in any case be adopted by the 6th month of pregnancy, as it can be serious impact on your baby and in particular on its circulation and kidneys, even if a single dose, and even if the pregnancy is at the end of its normal period.Tova medicine passes into breast milk. As a precaution, it is better to avoid its use during lactation.
 
Does this medicine influence on the ability to drive and use machines?
In rare cases, this medicine may cause dizziness and drowsiness.
 
 
AND METHOD OF ADMINISTRATION
rectal
 
 
DURATION OF TREATMENT
MUST ALWAYS BE STRICTLY OBSERVED your doctor's prescription.
 
What you need to know in case of an overdose?
In case of overdose or accidental poisoning should immediately call a doctor.
 
- Signs of intoxication
Suppository formulation limit the risk of overdose.
Usually symptoms of acute intoxication with niflumic acid is benign. The most commonly observed symptoms of gastrointestinal irritation. Other observed disturbances are expressed in drowsiness (5% of cases), headache. Patient who ingested 7.5 g niflumic acid, developed acute glomerulonephritis, which has passed without complications.
 
What side effects may occur during treatment?
As with all active members PRODUCTS This medicine may in some individuals lead to heavier or lighter SIDE EFFECTS.
In rare cases, however, some effects are seriozni.Lechenieto should be stopped immediately and inform your doctor in the following cases: allergic reactions:
influence on the skin, ie itching, rash, severe skin reactions when exposed to sunlight or ultraviolet rays; mehuropodobni rare disorder of the mucous membranes or skin effect on the lungs, ie asthma attacks; summarized as allergic shock gastrointestinal bleeding (vomiting blood or stool color black) These effects are more pronounced when doses are higher. In addition, in some cases, ulceration and perforation of the duodenum.
* Some other influences required to inform your doctor. Only he can decide on the action to be taken in cases of:
- Digestive disorders such as abdominal pain, vomiting or nausea.
* Some cases of changes in the bones (fluorosis) were observed following treatment with high doses for several years.
* Some changes in the results of laboratory tests may require analysis of blood or the liver or kidneys.
 
YOUR DOCTOR if you notice any side effects not listed in this leaflet.
 
 
How should I store the medication?
Suppositories are stored below 25 ° C, out of reach of children.
Do not use after the expiry date stated on the packaging.