Nidal Fort 75mg Ampharco Treatment Treatment of rheumatoid arthritis (3 blisters x 10 tablets)

Dosage form Box of 3 blisters x 10 tablets
Specifications Ketoprofen

Ingredient

Composition informationContent
Ketoprofen75mg

Uses

indications

Nidal Fort is indicated in the following cases:

Treatment of rheumatoid arthritis and degenerative arthritis.

Acute gout treatment.

Treatment of pain in the following cases:

  • Pain related to the spine (such as ankylosis, back pain).
  • Acute muscle disease. Reduce fever. Anti -inflammatory properties obtained by the synthetic inhibitory effect of prostaglandin and leukotrien. Ketoprofen also has Bradykinin resistance and stabilizes the lysosom membrane. However, as with other NSAIDs, the mechanism of action of Ketoprofen is still unknown.

    Pharmacokinetics

    absorption

    Ketoprofen is quickly absorbed with peak plasma concentrations achieved after 0.5 - 2 hours.

    Distribution

    Ketoprofen is widely linked to plasma proteins (> 99%), mainly albumin. The distribution volume is about 0.1L/kg.

    Metabolism

    The main metabolism of ketoprofen is associated with glucuronic acid.

    Elimination

    The semi -discharged time of plasma after drinking is 2-4 hours, about 80% of ketoprofen's doses are excreted in the urine within 24 hours, in the form of glucuronic metabolism.

  • Before taking Nidal Fort 75mg Ampharco Treatment Treatment of rheumatoid arthritis (3 blisters x 10 tablets)

    How to use

    Nidal Fort should take medicine during or immediately after meals.

    Dosage

    for pain, inflammation or acute muscle diseases:

    Dosage 50 - 100mg, 2-3 times/day.

    For economic system:

    Take the dose of 50mg, up to 3 times/day when needed.

    For people with kidney failure or liver failure:

    Should reduce the dose from 33% to 50% of the usual dose.

  • mild renal failure: maximum 150mg/day.
  • Moderate kidney failure: maximum 100mg/day

    Note: The above dose is for reference only. Specific dosage depends on the condition and level of progression of the disease. For a suitable dose, you need to consult a doctor or medical specialist.What to do when overdose? Gastrointestinal bleeding, hypotension, hypertension, or acute renal failure may occur, but very dangerous.

    There is no specific antidote. Patients should be treated for symptoms and support treatment after overdose NSAID.

    What to do when you forget a dose? However, if close to the next dose, skip the forgotten dose and take the next dose at the time as planned. Note that it should not be used double the prescribed dose.

  • Side Effects

    When using Nidal Fort, you may experience unwanted effects (ADR).

    Common, 1/100

  • Digestive: indigestion, nausea, abdominal pain, vomiting.
  • Uncommon, 1/1,000

  • Neurological: headache, dizziness, drowsiness.
  • digestive: constipation, diarrhea, flatulence, gastritis.
  • Skin and subcutaneous tissue: rash, itching.
  • body: edema, fatigue.
  • Rare, 1/10,000

  • Blood and lymphatic system: hemorrhagic anemia, anemia due to bleeding.
  • The immune system: anaphylactic reaction (including shock).
  • Neurological: Perception.
  • eyes: visual disorders like blurred vision.
  • ears and snails: tinnitus.
  • Respiratory system, chest and mediastinum: asthma, asthma attacks.
  • digestive: stomach stomatitis, stomach ulcer. Hepatitis: Hepatitis, increased transaminase, high serum bilirubin due to hepatitis
  • Unknown frequency:

  • Blood and lymphatic system: grain leukemia, thrombocytopenia, bone marrow failure, neutropenia.
  • Mental disorders: mood change.
  • Neurological: convulsions, taste disorders, depression, confusion, hallucinations, dizziness, discomfort, chicken sleep, reports on aseptic meningitis (especially in patients with autoimmune diseases such as systemic lupus, mixed connective tissue disease) with symptoms such as stiff neck, headache, nausea, vomiting, fever or loss.
  • Eyes: optic neuritis.
  • heart: heart failure, edema.
  • blood vessels: high blood pressure, vasodilation.
  • Respiratory, chest and mediastinum: Bronchospasm (especially in patients with hypersensitivity to aspirin and other NSAID drugs), rhinitis, allergic reactions for unknown causes, shortness of breath.
  • digestive: Exacection of colitis and Crohn's disease, hemorrhage and puncture of the digestive tract, stomach pain, black stool, vomiting blood, gastric bleeding can sometimes cause death, especially in the elderly.
  • Liver: abnormalities of liver function, jaundice.
  • Skin and subcutaneous tissue: sensitive to light, hair vibration, urticaria, angioedema, water polishing include Steven-Johnson syndrome and toxic skin necrosis, peeling skin and water peeling (including skin necrosis, diverse roses, hemorrhage.

    Kidney and urinary system: Acute renal failure, interstitial renal tubular inflammation, nephritis syndrome, kidney function abnormalities.

  • Systemic: headache, taste disorders. Clinical and epidemiological data shows that the use of NSAID drugs (especially high doses in a long time) may be related to an increase in the risk of arterial thrombosis (such as myocardial infarction or stroke).
  • Instructions on how to handle ADR

    When experiencing side effects of the drug, it is necessary to stop using and notify the doctor or go to the nearest medical facility for timely treatment.

    Warnings

    Before using the drug you need to read the instructions carefully and refer to the information below.

    contraindicated

    Nidal Fort is contraindicated in the following cases:

  • Hypersensitivity to ketoprofen or any ingredients of the drug.
  • Patients with asthma, urticaria or allergic reactions caused by aspirin or other NSAID drugs.

  • Pregnant women in the last three months of pregnancy.
  • Progressive peptic ulcer.

  • Children under 15 years old.
  • Severe heart failure.

    Severe liver failure

    Severe kidney failure

    Pain before and after surgery in coronary artery surgery (CABG).

    Caution when using

    Using the lowest dose effectively in the shortest time helps minimize unwanted effects.

    Because of the risk of bleeding, not using ketoprofen to treat pain associated with discreet bleeding (pain after the accident) or pain associated with trauma in the central nervous system.

    impaired cardiovascular, kidney and liver function

    When starting to treat, closely monitor kidney function in patients with heart failure, abnormalities of liver function, cirrhosis and kidney damage, patients are taking diuretics, patients with chronic renal insufficiency, especially in the patient who is the elderly. In these patients, using ketoprofen can reduce blood to the kidneys due to prostaglandin inhibition and lead to kidney decomposition.

    NSAID drugs have also been reported to toxicity in many different forms and this can lead to interstitial nephritis, nephrotic syndrome and kidney failure.

    In patients with abnormal liver function tests or a history of liver disease, it is advisable to evaluate the periodic transaminase level, especially when long -term treatment. Jaundice and rare hepatitis have been described when using ketoprofen.

    Effects on cardiovascular and cerebrovascular

    Need to monitor and advise appropriately for patients with a history of hypertension and/or have mild congestive heart failure to medium because the water retention and edema have been reported when the therapy coordinates with NSAID.

    Clinical and epidemiological testing data shows that the use of some NSAIDs (especially when taking high doses in a long time) may be related to an increase in the risk of arterial thrombosis (such as myocardial infarction, stroke). There is no enough data to eliminate the risk due to ketoprofen.

    Patients with hypertension, congestive heart failure, ischemia, untreated peripheral vascular disease and/or brain blood vessels should only be treated with ketoprofen after careful consideration. Similarly, it is advisable to consider before starting long -term treatment in patients at risk of cardiovascular disease (e.g. hypertension, increased blood fat, diabetes, smoking).

    Respiratory disorders

    Patients with asthma with chronic rhinitis, chronic sinusitis, and/or nasal polyps are at risk of allergies to aspirin and/or higher NSAID drugs. When using this medication can cause asthma attacks or bronchospasm, especially in people who are allergic to aspirin or nsAID drugs.

    Bleeding, ulcers and digestive puncture

    Hemorrhage, ulcers and digestive perforation can lead to deaths that have been reported to all NSAID drugs at any time of the treatment process, with or without warning symptoms or a history of serious events in the digestive tract.

    Some evidence of epidemiology shows that Ketoprofen may be related to a high risk of serious digestion, as well as other NSAID drugs, especially in high doses.

    The risk of bleeding, ulcers and digestive perforation when increasing the dose of NSAID drugs, in patients with a history of ulcer, especially when bleeding or perforation, and in the elderly.

    Older patients start treatment with the lowest possible dose. Treatment in combination with digestive protection drugs (such as Misoprostol or proton pump inhibitors) should be considered in these patients, and for patients to use simultaneously with low -dose aspirin, or other drugs that increase the risk for the digestive tract. Ketoprofen should not be used for patients with a history of gastrointestinal ulcer.

    Use NSAID caution in patients with a history of digestive disease (such as ulcerative colon, Crohn's disease) because it can cause disease outbreaks.

    Patients with a history of gastrointestinal toxicity, especially when older, should report abdominal abdominal signs (especially digestive bleeding), in the first stage of treatment.

    Be cautious when used for patients who use simultaneous drugs at risk of ulcers or other bleeding such as oral corticosteroids, or anticoagulants such as warfarin, selective inhibitors of Serotonin reabsorption or platelet anti -platelet -like anti -platelet -like drugs.

    When bleeding or gastrointestinal ulcers in patients using ketoprofen, drugs should be discontinued.

    used for children

    Safety and effectiveness in children have not been recorded.

    Used for older people

    As with any type of NSAID, should be careful when treating the elderly (65 years or older).

    The ability to drive and operate machines

    using ketoprofen can make patients feel dizzy, drowsiness and affect vision. Therefore, patients should not drive or operate the machine, unless the patient assesses the effect of the drug on their bodies, as well as the patient can perform those activities safely.

    Pregnancy

    Prostaglandin synthesis inhibitors can adversely affect pregnancy and/or embryo/fetal development. Data from epidemiological studies shows an increase in the risk of miscarriage, heart defects and abdominal cracks (gastroschisis) after using Prostaglandin synthetic inhibitors at the beginning of pregnancy.

    The absolute risk of cardiovascular defects increases from less than 1% to about 1.5%. This risk is thought to be due to increased dose and treatment time. In the first three months and three months between pregnancy, ketoprofen should not be used if not needed. If you have to use ketoprofen for women who are trying to conceive or in the first three months and three months in the middle of pregnancy, the dose should be kept low and the treatment time is as short as possible.

    During the last three months of pregnancy, all Prostaglandin synthetic inhibitors can cause the fetus:

  • Cardiac toxicity (due to early arteriosclerosis and pulmonary hypertension).
  • Renal dysfunction, which can lead to kidney failure due to low amniotic fluid.

    At the end of pregnancy, the mother and the fetus may be at risk of bleeding due to anti -platelet aggression effects of the drug, even if the dose is very low.

  • Inhibition of uterine spasms slows birth or prolonged pregnancy.
  • Therefore, ketoprofen is contraindicated in the last three months of pregnancy.

    The period of breastfeeding

    It is unclear whether the drug is excreted through breast milk or not. As with other medications excreted by breast milk, Ketoprofen is not recommended for breastfeeding women.

    Interactive drug

    anticoagulant drugs (such as heparin and warfarin) and anti -platelets (such as ticlopidin, clopidogrel):

    increases the risk of bleeding. If it is impossible to avoid simultaneously, should closely monitor patients.

    Li-ti:

    There is a risk of increased plasma concentrations in plasma, sometimes increasing to toxic concentrations, due to reduction in lip-tilled excretion | kidney. When needed, closely monitor Li-ti concentration in plasma and adjust the dose of li-ti during and after treatment with NSAID drugs.

    Other NSAID painkillers (including cyclooxygenase-2 inhibitors) and high doses of salicylate:

    Avoid simultaneous use of two or more NSAID drugs (including aspirin) because this can increase the side effects of 24 of the drug, especially ulcers or gastrointestinal bleeding.

    methotrexate:

    Serious drug interactions were recorded when US, high doses of methotrexate along with NSAID drugs, including ketoprofen, due to reduction of methotrexate excretion.

  • With a dose of over 15mg/week: The risk of blood toxicity of methotrexate increases, especially when taking high doses (> 15mg/week), may be associated with the occupation of methotrexate associated with protein and its reduction in the kidneys. If there is any change in kidney function or if the patient is the elderly, the monitor must be done more often.
  • Mifepriston:

    Do not take NSAID drugs for about 8-12 days after using Mifepriston because NSAID drugs can reduce the effectiveness of Mifepriston.

    pentoxifyllin:

    Increased risk of bleeding. Clinical monitoring more often and tracking bleeding time is necessary.

    Hematoplastic drugs (Beta blockers inhibitors inhibitors, diuretics):

    There is a risk of reducing the effectiveness of antihypertensive drugs (due to nsaids inhibiting vascular dilatation ability of prostaglandin).

    Diuretics:

    There is a risk of reducing the effectiveness of diuretics. Patients and especially patients dehydrated due to use | Diuretics are at higher risk of secondary renal failure due to reduced renal perfusion due to prostaglandin inhibition. For these patients, it is necessary to rehydrate before starting a combination therapy and monitoring the kidney function at the beginning of treatment.

    heart glycosides:

    NSAID drugs can cause heart failure, reduce glomerular filtration and increase heart glycosides in plasma.

    ciclosporin:

    Increased the risk of glomerular poisoning, especially in the elderly. Corticosteroids: Increased risk of ulcerative or gastrointestinal bleeding.

    Quinolon antibiotics:

    Animal research data indicates that NSAID drugs may increase the risk of convulsions when used with Quinolon antibiotics. Patients using NSAID and Quinolon antibiotics may increase the risk of convulsions.

    tacrolimus:

    There may be risk of kidney poisoning when shared with NSAID with Tacrolimus, especially on the elderly.

    Probenecid:

    Concentrated with probenecid may significantly reduce the clearance in the plasma of ketoprofen.

    Transfer inhibitors and Angiotensin II:

    In patients with renal function damage (such as dehydration or elderly), simultaneously taking transferred enzyme inhibitors or Angiotensin II anti-drugs with Cycloxygenase-2 inhibitors can lead to further impairment of kidney function, including acute renal failure.

    zidovudin:

    Increased risk of hematopology when using NSAID with zidovudin. There is evidence that the risk of joint hematoma and hematoma in patients with coagulation disorders (HAemophilia) HIV (+) is treated simultaneously zidovudine and ibuprofen.

    Storage

    at temperatures below 30 ° C. Avoid direct light and wet place.

    Other drugs

    Disclaimer

    Every effort has been made to ensure that the information provided by Drugslib.com is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Drugslib.com information has been compiled for use by healthcare practitioners and consumers in the United States and therefore Drugslib.com does not warrant that uses outside of the United States are appropriate, unless specifically indicated otherwise. Drugslib.com's drug information does not endorse drugs, diagnose patients or recommend therapy. Drugslib.com's drug information is an informational resource designed to assist licensed healthcare practitioners in caring for their patients and/or to serve consumers viewing this service as a supplement to, and not a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.

    The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. Drugslib.com does not assume any responsibility for any aspect of healthcare administered with the aid of information Drugslib.com provides. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

    count views

    Popular Keywords