Medication info
Meloxicam Capsules (Meloxicam)

Meloxicam Capsules (Meloxicam)

Prescription medicationHard capsuleOral
Ingredient · strength
Meloxicam›7.5mg / 1 capsule
Manufacturer / importer
Celix Co., Ltd.
Appearance
A hard capsule with a greenish-brown upper and lower part filled with yellow powder
Packaging
30 capsules/bottle, 300 capsules/bottle
Approval status
Active

MFDS item code 200411043 · Notified 2004.11.25 · Insurance code 646200850

Summary

Main use
Relief of symptoms of rheumatoid arthritis, ankylosing spondylitis, and acute exacerbations of osteoarthritis (short-term)
Who takes it
Adults
Adult dose
1. Acute exacerbation of osteoarthritis (degenerative joint disease): ○ Adults: Administer 7.5 mg of meloxicam orally once daily. If symptoms do not improve, the dose may be increased 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 according to the response to treatment. Do not administer more than 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 failure undergoing hemodialysis should not receive more than 7.5 mg daily.

Ingredients

Manufacturer
Celix Co., Ltd.

Efficacy & effects

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

  • Pain
  • impaired movement
View approved original text

This medication is effective for short-term symptom relief during the acute exacerbation of osteoarthritis, accompanied by pain and movement disorder. It is also used to improve symptoms caused by rheumatoid arthritis and ankylosing spondylitis, thus helping to effectively treat the discomfort associated with inflammatory diseases related to joints.

How to take

Adult dose

1. Acute exacerbation of osteoarthritis (degenerative joint disease): ○ Adults: Administer 7.5 mg of meloxicam orally once daily. If symptoms do not improve, the dose may be increased 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 according to the response to treatment. Do not administer more than 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 failure undergoing hemodialysis should not receive more than 7.5 mg daily.

Precautions

This medication can cause gastrointestinal bleeding if taken regularly by individuals who consume more than three drinks daily, so consultation with a doctor or pharmacist is essential. This medication may increase the risk of cardiovascular diseases, so individuals at risk of heart disease or stroke should exercise particular caution, and if symptoms such as chest pain or shortness of breath occur while taking it, the medication should be discontinued immediately. This medication can cause severe gastrointestinal side effects such as gastrointestinal bleeding, ulcers, or perforations, so those with a history of gastrointestinal diseases or the elderly should use it with extra caution. Severe skin reactions such as exfoliative dermatitis, Stevens-Johnson syndrome, and toxic epidermal necrolysis can occur, so if any skin abnormalities arise, the medication should be discontinued immediately and medical attention should be sought. Since it may affect liver and kidney function, it is necessary to check for liver or kidney diseases before taking this medication and to have regular tests during use. Women planning to become pregnant or those who may become pregnant should avoid using this medication, as it may affect fertility. This medication can be dangerous for those with certain allergic reactions or asthma, so individuals who have previously shown allergic reactions to non-steroidal anti-inflammatory drugs should not take it. Patients with chronic conditions such as hypertension, heart failure, or kidney disease should closely monitor their condition while taking this medication and follow their doctor's instructions. The risk of side effects may increase when used in combination with other non-steroidal anti-inflammatory drugs, anticoagulants, diuretics, etc., so consultation with a doctor before use is required. When taking this medication, it is advised to use the smallest dose possible for the shortest duration. Regular blood tests and liver and kidney function tests are necessary during long-term use. Dizziness, drowsiness, visual disturbances may occur during treatment; hence, caution is advised when driving or operating machinery. In cases of overdose, serious side effects such as gastrointestinal bleeding, acute kidney failure, or heart problems may occur; hence, the prescribed dosage must be adhered to, and in case of overdose, medical institutions should be contacted immediately. This medication should be kept out of reach of children and stored in its original container to prevent misuse or degradation of quality.

Side effects

  • Gastrointestinal bleeding
  • cardiovascular thromboembolic response
  • myocardial infarction
  • stroke
  • bleeding from the stomach or intestines
  • ulcer
  • perforation
  • exfoliative dermatitis
  • mucocutaneous syndrome
  • toxic epidermal necrolysis
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  • anaphylactic reaction
  • interstitial nephritis
  • glomerulonephritis
  • renal medullary necrosis
  • nephrotic syndrome
  • elevation of serum transaminases
  • elevation of liver function tests
  • increase in plasma creatinine
  • increase in blood urea nitrogen
  • aplastic anemia
  • bone marrow suppression
  • changes in blood cell count
  • leukopenia
  • thrombocytopenia
  • anemia
  • decrease in plasma iron
  • decrease in hemoglobin
  • decrease in hematocrit
  • neutrophilia
  • eosinophilia
  • basophilia
  • monocytosis
  • agranulocytosis
  • anaphylaxis
  • anaphylactoid reaction
  • malaise
  • confusion
  • loss of orientation
  • mood changes
  • mood disorders
  • insomnia
  • nightmares
  • anxiety
  • increased appetite
  • depression
  • neuro-irritability
  • dizziness
  • drowsiness
  • headache
  • cranial pressure
  • fatigue
  • lethargy
  • taste dysfunction
  • mental confusion
  • seizures
  • sensory disturbances
  • tremors
  • blurred vision
  • conjunctivitis
  • foreign body sensation in the eye
  • scleral hemorrhage
  • 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
  • anorexia
  • peptic ulcer
  • occult gastrointestinal bleeding
  • gross gastrointestinal bleeding
  • stomatitis
  • gastritis
  • esophagitis
  • belching
  • dry mouth
  • thirst
  • angular cheilitis
  • occult blood in stool
  • gastrointestinal perforation
  • colitis
  • pancreatitis
  • melena
  • perforated peptic ulcer
  • hepatitis
  • elevated plasma transaminase levels
  • elevated bilirubin
  • jaundice
  • liver failure
  • alopecia
  • increased sweating
  • skin rash
  • urticaria
  • pruritus
  • angioedema
  • vesicular dermatitis
  • erythema multiforme
  • photosensitivity reaction
  • contact dermatitis
  • fixed drug eruption
  • urinary disorder
  • elevated plasma creatinine levels
  • elevated urea levels
  • decreased total protein
  • decreased albumin
  • proteinuria
  • glucosuria
  • increased urinary sediment
  • hematuria
  • sodium and fluid retention
  • hyperkalemia
  • acute renal failure
  • decreased urine output
  • frequent urination
  • urinary tract infection
  • interstitial nephritis
  • edema
  • lower extremity edema
  • fatigue
  • fever
  • facial edema
  • syncope
  • weight loss
  • weight gain
  • axillary and breast pain
  • arthralgia
  • low back pain
  • axillary and chest pain
  • stiffness
  • lower limb weakness
  • decreased female reproductive capacity
  • dehydration
  • drowsiness
  • nausea
  • vomiting
  • epigastric pain
  • hypertension
  • acute renal failure
  • liver failure
  • respiratory depression
  • coma
  • seizures
  • cardiovascular collapse
  • cardiac arrest

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

Storage

This medication should be stored in a special container that does not allow light to enter, as it is light-sensitive. It is also important to maintain a temperature between 1 to 30 degrees Celsius during storage to safely preserve the medication's effectiveness.

Appearance and packaging

Appearance

A hard capsule with a greenish-brown upper and lower part filled with yellow powder

Package unit

30 capsules/bottle, 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.