Medication info
Meloxicam Capsule 15 mg (Meloxicam)

Meloxicam Capsule 15 mg (Meloxicam)

Prescription medicationHard capsuleOral
Ingredient · strength
Meloxicam›15mg / 1 capsule
Manufacturer / importer
NBK Pharmaceutical Co., Ltd.
Appearance
Hard capsule with a light yellow powder inside, greenish upper part, and yellow lower part
Packaging
For domestic use - 30 capsules/bottle, For domestic use - 300 capsules/bottle
Approval status
Active

MFDS item code 202004002 · Approved 2020.05.28

Summary

Main use
Treatment of rheumatoid arthritis, acute exacerbations of osteoarthritis (short-term), and symptoms of ankylosing spondylitis
Who takes it
Adults
Adult dose
1. During acute exacerbations of osteoarthritis (degenerative arthritis): ○ Adults: Administer 7.5 mg of meloxicam orally once daily. If symptoms do not improve, the dose may be increased to up to 15 mg daily as needed. 2. Rheumatoid arthritis, ankylosing spondylitis: ○ Adults: Administer 15 mg of this medicine orally once daily. The dose may be reduced to 7.5 mg daily depending on the response to treatment. Do not exceed 15 mg of this medicine per day. Take it with water or another beverage during a meal. ○ In elderly patients or those at increased risk of adverse reactions, treatment is usually initiated at a dose of 7.5 mg daily. ○ Patients with severe renal impairment receiving hemodialysis must not receive more than 7.5 mg daily.

Ingredients

Manufacturer
NBK Pharmaceutical Co., Ltd.

Efficacy & effects

Treatment of rheumatoid arthritis, acute exacerbations of osteoarthritis (short-term), and symptoms of ankylosing spondylitis

  • Pain
  • ataxia
  • acute exacerbation
  • symptoms
  • symptoms
  • symptoms
View approved original text

This medication helps to alleviate pain and ataxia during acute exacerbations of osteoarthritis (degenerative arthritis) in a short period. It also effectively treats symptoms caused by rheumatoid arthritis and ankylosing spondylitis. It is used to improve various inflammation and pain related to arthritis.

How to take

Adult dose

1. During acute exacerbations of osteoarthritis (degenerative arthritis): ○ Adults: Administer 7.5 mg of meloxicam orally once daily. If symptoms do not improve, the dose may be increased to up to 15 mg daily as needed. 2. Rheumatoid arthritis, ankylosing spondylitis: ○ Adults: Administer 15 mg of this medicine orally once daily. The dose may be reduced to 7.5 mg daily depending on the response to treatment. Do not exceed 15 mg of this medicine per day. Take it with water or another beverage during a meal. ○ In elderly patients or those at increased risk of adverse reactions, treatment is usually initiated at a dose of 7.5 mg daily. ○ Patients with severe renal impairment receiving hemodialysis must not receive more than 7.5 mg daily.

Precautions

This medication must be discussed with a doctor or pharmacist for individuals who regularly consume more than three glasses of alcohol daily, as taking it with alcohol increases the risk of gastrointestinal bleeding. This medication may increase the risk of cardiovascular diseases. Special caution should be exercised for those with a history of cardiovascular disease or risk factors, as serious cardiovascular problems like heart attacks or strokes may occur. If chest pain, shortness of breath, weakness, or slurred speech occurs while taking this, discontinue use immediately and consult a doctor. This medication can cause serious gastrointestinal adverse reactions such as gastrointestinal bleeding, ulcers, or perforations. Elderly patients or those with a history of gastrointestinal diseases should be particularly cautious, and if abdominal pain, blood in stool, or vomiting occurs, medical personnel should be informed immediately. This medication can cause severe allergic reactions on the skin. If symptoms such as rashes, mucosal damage, or severe itching occur, discontinue use immediately and consult medical personnel. This medication may affect kidney function; therefore, individuals with kidney disease or poor kidney function should be cautious during use. Liver function abnormalities may occur, so individuals with a history of liver disease or abnormal liver function test results should have their liver function checked regularly. Women planning to become pregnant should avoid this medication, and it should also be avoided by pregnant or breastfeeding women, as it may reduce reproductive ability. This medication is not to be administered to persons with certain allergic reactions, asthma patients, individuals with a history of gastrointestinal bleeding or ulcers, severe liver or kidney disease, or severe heart failure. Dizziness, drowsiness, and visual disturbances may occur while taking this medication, so caution is needed when driving or operating machinery. Since this medication interacts with many other drugs, it is essential to inform the doctor or pharmacist about any medications currently being taken, especially when combined with anticoagulants, diuretics, blood pressure medications, lithium, or methotrexate. When taking this medication, it is safest to use the minimum dosage and shortest duration possible. Regular blood tests and liver/kidney function tests are required for long-term use. In case of overdose, symptoms such as nausea, vomiting, drowsiness, gastrointestinal bleeding may appear, and in severe cases, renal failure, liver failure, or coma may occur; immediate medical attention should be sought. Keep out of reach of children, and storing the medication in its original packaging helps maintain its quality.

Side effects

  • Gastrointestinal bleeding
  • cardiovascular thrombotic response
  • myocardial infarction
  • stroke
  • bleeding from the stomach or intestines
  • ulcers
  • perforation
  • exfoliative dermatitis
  • Stevens-Johnson syndrome
  • toxic epidermal necrolysis
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  • anaphylactic reaction
  • interstitial nephritis
  • glomerulonephritis
  • medullary nephrosis
  • nephrotic syndrome
  • elevated serum transaminases
  • increased liver function tests
  • elevated plasma creatinine
  • increased blood urea nitrogen
  • aplastic anemia
  • bone marrow suppression
  • changes in blood cell counts
  • leukopenia
  • thrombocytopenia
  • anemia
  • decreased plasma iron
  • decreased hemoglobin
  • decreased hematocrit
  • increased neutrophils
  • increased eosinophils
  • increased basophils
  • increased monocytes
  • agranulocytosis
  • anaphylaxis
  • discomfort
  • confusion
  • loss of directional sense
  • mood changes
  • mood disorders
  • insomnia
  • nightmares
  • anxiety
  • increased appetite
  • depression
  • hyperexcitability
  • dizziness
  • drowsiness
  • headache
  • cranial discomfort
  • fatigue
  • lethargy
  • dysgeusia
  • mental confusion
  • seizures
  • sensory disturbances
  • tremors
  • blurred vision
  • conjunctivitis
  • foreign body sensation in the eye
  • hemorrhage in the eye
  • tinnitus
  • palpitations
  • elevated blood pressure
  • flushing
  • arrhythmia
  • tachycardia
  • hypotension
  • hypertension
  • myocardial infarction
  • angina pectoris
  • heart failure
  • vasculitis
  • cough
  • upper respiratory infection
  • asthma
  • bronchospasm
  • dyspnea
  • dyspepsia
  • nausea
  • vomiting
  • abdominal pain
  • constipation
  • bloating
  • diarrhea
  • loss of appetite
  • peptic ulcer
  • occult gastrointestinal bleeding
  • visible gastrointestinal bleeding
  • stomatitis
  • gastritis
  • esophagitis
  • belching
  • dry mouth
  • thirst
  • angular cheilitis
  • occult blood in stool
  • gastrointestinal perforation
  • colitis
  • pancreatitis
  • melena
  • perforated peptic ulcer
  • hepatitis
  • jaundice
  • liver failure
  • alopecia
  • increased sweating
  • skin rash
  • urticaria
  • angioedema
  • vesicular dermatitis
  • erythema multiforme
  • photosensitivity reactions
  • contact dermatitis
  • fixed drug eruption
  • urinary retention
  • elevated plasma creatinine
  • increased urea levels
  • decreased total protein
  • decreased albumin
  • proteinuria
  • glucosuria
  • increased urine sediment
  • hematuria
  • sodium retention
  • fluid retention
  • hyperkalemia
  • acute renal failure
  • decreased urine output
  • frequency of urination
  • urinary tract infection
  • interstitial nephritis
  • edema
  • lower limb edema
  • lethargy
  • fever
  • facial swelling
  • syncope
  • weight loss
  • weight gain
  • axillary pain
  • breast pain
  • arthralgia
  • back pain
  • chest pain
  • stiffness
  • weakness in lower extremities
  • decreased female reproductive capacity
  • dehydration

Not everyone experiences these, and they can vary from person to person.

Storage

This medication is sensitive to light and should be kept in a lightproof container. Additionally, it is recommended to store it at room temperature between 1 and 30 degrees Celsius to maintain its effectiveness.

Appearance and packaging

Appearance

Hard capsule with a light yellow powder inside, greenish upper part, and yellow lower part

Package unit

For domestic use - 30 capsules/bottle, For domestic use - 300 capsules/bottle

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.

Questions about this medicine

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This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.