Medication info

Meloxone Capsule 7.5 mg (Meloxicam)

Prescription medicationOralExpired
Ingredient · strength
Meloxicam›7.5mg / 1 capsule
Manufacturer / importer
Seohung Co., Ltd.
Appearance
Light yellow powder in a hard capsule with a pale green shell
Packaging
30 capsules/bottle, 300 capsules/bottle
Approval status
Expired

MFDS item code 202002677 · Approved 2020.04.16

This product's status changed to Expired on 2025.04.16. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Relief of symptoms of rheumatoid arthritis, acute exacerbations of osteoarthritis, and ankylosing spondylitis
Who takes it
Adults
Adult dose
Acute exacerbation 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 15 mg daily as needed. Rheumatoid arthritis, ankylosing spondylitis: Adults: Administer 15 mg of this drug orally once daily. The dose may be reduced to 7.5 mg daily according to response to treatment. Do not administer more than 15 mg of this drug daily. Take 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 undergoing hemodialysis should not receive more than 7.5 mg daily.

Ingredients

Manufacturer
Seohung Co., Ltd.

Efficacy & effects

Relief of symptoms of rheumatoid arthritis, acute exacerbations of osteoarthritis, and ankylosing spondylitis

  • Pain
  • movement impairment
  • acute exacerbation of osteoarthritis
  • symptoms of rheumatoid arthritis
  • symptoms of ankylosing spondylitis
View approved original text

This medication is used for the short-term relief of symptoms during acute exacerbations of osteoarthritis associated with pain and mobility impairment. It also treats symptoms of rheumatoid arthritis and ankylosing spondylitis, reducing discomfort for patients. In summary, this drug helps effectively improve symptoms of various inflammatory diseases related to arthritis. Therefore, it is actively used for alleviating joint pain and inflammation.

How to take

Adult dose

Acute exacerbation 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 15 mg daily as needed. Rheumatoid arthritis, ankylosing spondylitis: Adults: Administer 15 mg of this drug orally once daily. The dose may be reduced to 7.5 mg daily according to response to treatment. Do not administer more than 15 mg of this drug daily. Take 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 undergoing hemodialysis should not receive more than 7.5 mg daily.

Precautions

This medication should be consulted with a doctor or pharmacist if taken by individuals who regularly consume more than three glasses of alcohol daily due to increased risk of gastrointestinal bleeding. This medication may increase the risk of cardiovascular problems such as myocardial infarction or stroke in individuals with cardiovascular diseases or risk factors. If symptoms arise, discontinue use immediately and seek medical attention. This medication can cause serious gastrointestinal side effects such as gastrointestinal bleeding, ulcers, and perforation, and caution is particularly necessary for the elderly and individuals with a history of gastrointestinal diseases. Severe allergic skin reactions or dermatitis may occur, so if symptoms such as skin rash or mucosal lesions appear, discontinue use immediately. This medication may affect kidney and liver function, so individuals with existing kidney or liver diseases should consult a doctor before taking it and require regular check-ups during use. Women who are pregnant or planning to become pregnant should not take this medication, and breastfeeding women should also avoid it. This medication may cause serious side effects in individuals with certain genetic metabolic disorders; therefore, those with lactose intolerance and similar conditions should not take it. The risk of side effects increases when this medication is taken with other non-steroidal anti-inflammatory drugs, so it should be avoided. Strict management by a doctor is needed when taken with anticoagulants, lithium, methotrexate, etc. Elderly patients may have reduced kidney, liver, and heart function, so it should be taken carefully at a minimum dose, with close monitoring for side effects. Overdose of this medication can cause symptoms such as vomiting, drowsiness, and gastrointestinal bleeding; in severe cases, it may lead to life-threatening conditions such as kidney failure, liver failure, or seizures, requiring immediate emergency treatment.

Side effects

  • Gastrointestinal bleeding
  • cardiovascular thrombotic reactions
  • myocardial infarction
  • stroke
  • bleeding of the stomach or intestines
  • ulcers
  • perforation
  • exfoliative dermatitis
  • Stevens-Johnson syndrome
  • toxic epidermal necrolysis
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  • anaphylactic reactions
  • interstitial nephritis
  • glomerulonephritis
  • renal medullary necrosis
  • nephrotic syndrome
  • elevated serum transaminases
  • increased liver function tests
  • increased plasma creatinine
  • elevated blood urea nitrogen
  • aplastic anemia
  • bone marrow suppression
  • changes in blood cell counts
  • leukopenia
  • thrombocytopenia
  • anemia
  • decreased plasma iron
  • decreased hemoglobin
  • reduced hematocrit
  • increased neutrophils
  • increased eosinophils
  • increased basophils
  • increased monocytes
  • agranulocytosis
  • anaphylaxis
  • anaphylactoid reactions
  • malaise
  • confusion
  • loss of orientation
  • mood changes
  • mood disorders
  • insomnia
  • nightmares
  • anxiety
  • increased appetite
  • depression
  • irritability
  • dizziness
  • drowsiness
  • headache
  • head discomfort
  • fatigue
  • lassitude
  • taste dysfunction
  • mental confusion
  • seizures
  • sensory disturbances
  • tremors
  • blurred vision
  • conjunctivitis
  • foreign body sensation in the eye
  • subconjunctival hemorrhage
  • tinnitus
  • palpitations
  • elevated blood pressure
  • flushing
  • facial flushing
  • arrhythmia
  • tachycardia
  • hypotension
  • hypertension
  • myocardial infarction
  • angina
  • heart failure
  • vasculitis
  • cough
  • upper respiratory tract infection
  • asthma
  • bronchial spasm
  • dyspnea
  • dyspepsia
  • nausea
  • vomiting
  • abdominal pain
  • constipation
  • abdominal distension
  • diarrhea
  • anorexia
  • peptic ulcer
  • occult gastrointestinal bleeding
  • gross gastrointestinal bleeding
  • stomatitis
  • gastritis
  • esophagitis
  • belching
  • dry mouth
  • thirst
  • angular cheilitis
  • occult blood in stools
  • gastric perforation
  • colitis
  • pancreatitis
  • melena
  • perforated peptic ulcer
  • hepatitis
  • jaundice
  • hepatic failure
  • alopecia
  • skin rash
  • urticaria
  • itching
  • 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
  • glycosuria
  • increased urinary sediment
  • hematuria
  • sodium and fluid retention
  • hyperkalemia
  • acute renal failure
  • decreased urine output
  • frequent urination
  • urinary tract infection
  • interstitial nephritis
  • edema
  • lower limb swelling
  • malaise
  • fever
  • facial edema
  • syncope
  • weight loss
  • weight gain
  • axillary and breast pain
  • arthralgia
  • low back pain
  • axillary and chest pain
  • stiffness
  • weakness in the lower limbs
  • reduced reproductive capacity in women
  • dehydration
  • drowsiness
  • nausea
  • vomiting
  • epigastric pain
  • hypertension
  • acute renal failure
  • hepatic 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 container that blocks light and air, preferably at room temperature between 1 and 30 degrees Celsius. Proper storage can prolong the medication's effectiveness.

Appearance and packaging

Appearance

Light yellow powder in a hard capsule with a pale green shell

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.

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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.