Medication info
Meloxicam Capsule 7.5mg (Meloxicam)

Meloxicam Capsule 7.5mg (Meloxicam)

Prescription medicationHard capsuleOral
Ingredient · strength
Meloxicam›7.5mg / 1 capsule
Manufacturer / importer
Joah Pharmaceutical Co., Ltd.
Appearance
Light yellow powder contained in hard capsules that are light green in color.
Packaging
30 capsules/bottle, 300 capsules/bottle
Approval status
Active

MFDS item code 201503642 · Approved 2015.06.08 · Insurance code 644603170

Summary

Main use
Relief of symptoms of rheumatoid arthritis, acute exacerbations of osteoarthritis (short-term use), and ankylosing spondylitis
Who takes it
Adults
Adult dose
1. Acute exacerbations of osteoarthritis (degenerative joint disease): ○ Adults: Administer meloxicam 7.5 mg 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 depending on 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 receiving hemodialysis should not receive more than 7.5 mg daily.

Ingredients

Manufacturer
Joah Pharmaceutical Co., Ltd.

Efficacy & effects

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

  • Pain
  • motor dysfunction
  • osteoarthritis
  • acute exacerbation
  • rheumatoid arthritis
  • ankylosing spondylitis
View approved original text

This medication helps relieve pain and functional impairment in cases of acute exacerbation of osteoarthritis in a short period. It also effectively treats inflammatory and pain symptoms associated with rheumatoid arthritis and ankylosing spondylitis. Thus, it is used to manage pain and inflammation caused by arthritis, improving discomfort in daily life.

How to take

Adult dose

1. Acute exacerbations of osteoarthritis (degenerative joint disease): ○ Adults: Administer meloxicam 7.5 mg 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 depending on 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 receiving hemodialysis should not receive more than 7.5 mg daily.

Precautions

This medication may cause an increased risk of gastric bleeding for individuals who consume three or more alcoholic beverages daily, and therefore it is essential to consult a doctor or pharmacist. This medication can cause cardiovascular issues; individuals at risk for heart diseases or strokes must exercise caution, and if symptoms like chest pain or dyspnea arise, discontinue use immediately. This medication may lead to serious gastrointestinal issues such as bleeding, ulcers, or perforation, and particular care should be taken by elderly individuals or those with a history of gastrointestinal diseases. Severe allergic reactions or dermatitis may occur, so if any abnormal skin symptoms arise, discontinue use immediately. Rarely, this medication can cause renal issues, so individuals with reduced kidney function should be monitored closely. It may temporarily worsen liver function, so individuals with liver diseases or abnormal liver function test results should consult a doctor before use. This medication may reduce female fertility, so women planning to become pregnant should refrain from using it. Individuals with allergic reactions or hypersensitivity to aspirin or other NSAIDs should not take this medication. This medication should not be used by patients with gastrointestinal bleeding, ulcers, severe hepatic impairment, kidney failure, heart failure, severe hypertension, adolescents under 15 years old, and women who are pregnant or breastfeeding. While on this medication, symptoms such as gastrointestinal issues, skin abnormalities, and renal function decline should be monitored closely, and any unusual symptoms should be promptly discussed with healthcare professionals. This medication may interact with other drugs, so inform your doctor of any other medications currently being taken. Pregnant women should not take this medication, especially in the later stages of pregnancy, as it can seriously affect the fetus. Breastfeeding women should also refrain from using this medication for safety. Elderly patients have a higher risk of side effects due to weakened kidney and liver function and should take the minimal effective dose with caution. Overdosage may result in symptoms such as nausea, vomiting, drowsiness, and in severe cases, renal failure or cardiac issues, necessitating immediate medical attention. Store this medication out of reach of children and keep it in its original container for safety.

Side effects

  • Gastrointestinal bleeding
  • cardiovascular thrombotic reactions
  • myocardial infarction
  • stroke
  • bleeding from the stomach or intestines
  • ulcers
  • perforations
  • exfoliative dermatitis
  • mucous membrane syndrome
  • toxic epidermal necrolysis
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  • anaphylactic reactions
  • interstitial nephritis
  • glomerulonephritis
  • renal medullary necrosis
  • nephrotic syndrome
  • elevated serum transaminases
  • elevated liver function tests
  • increased plasma creatinine
  • elevated blood urea nitrogen
  • aplastic anemia
  • bone marrow suppression
  • changes in blood cell count
  • leukopenia
  • thrombocytopenia
  • anemia
  • decreased plasma iron
  • reduced hemoglobin
  • decreased hematocrit
  • increased neutrophils
  • increased eosinophils
  • increased basophils
  • increased monocytes
  • agranulocytosis
  • anaphylaxis
  • malaise
  • confusion
  • loss of directional sense
  • mood changes
  • mood disorders
  • insomnia
  • nightmares
  • anxiety
  • increased appetite
  • depression
  • irritability
  • dizziness
  • drowsiness
  • headache
  • intracranial pressure
  • fatigue
  • lethargy
  • taste function disorder
  • mental confusion
  • seizures
  • sensory disturbance
  • tremors
  • blurred vision
  • conjunctivitis
  • foreign body sensation in the eye
  • subconjunctival hemorrhage
  • tinnitus
  • palpitations
  • elevated blood pressure
  • flushing
  • arrhythmia
  • tachycardia
  • hypotension
  • hypertension
  • myocardial infarction
  • angina pectoris
  • heart failure
  • vasculitis
  • cough
  • upper respiratory tract infection
  • asthma
  • bronchospasm
  • shortness of breath
  • dyspepsia
  • nausea
  • vomiting
  • abdominal pain
  • constipation
  • bloating
  • diarrhea
  • decreased appetite
  • peptic ulcers
  • occult gastrointestinal bleeding
  • macroscopic gastrointestinal bleeding
  • stomatitis
  • gastritis
  • esophagitis
  • belching
  • dry mouth
  • thirst
  • angular cheilitis
  • occult blood in stools
  • gastrointestinal perforation
  • colitis
  • pancreatitis
  • melena
  • perforated peptic ulcer
  • hepatitis
  • elevated plasma transaminase levels
  • increased bilirubin
  • jaundice
  • hepatic failure
  • alopecia
  • increased sweating
  • skin rash
  • urticaria
  • itching
  • angioedema
  • vesicular dermatitis
  • erythema multiforme
  • photosensitivity reactions
  • contact dermatitis
  • fixed drug eruption
  • urination disorders
  • elevated plasma creatinine levels
  • increased urea levels
  • total protein decrease
  • decreased albumin
  • proteinuria
  • glucosuria
  • increased urinary sediment
  • hematuria
  • sodium and fluid retention
  • hyperkalemia
  • acute renal failure
  • decreased urine output
  • frequency of urination
  • urinary tract infection
  • interstitial nephritis
  • edema
  • peripheral edema
  • fatigue
  • fever
  • facial swelling
  • syncope
  • weight loss
  • weight gain
  • armpit and breast pain
  • arthralgia
  • low back pain
  • chest and armpit pain
  • stiffness
  • weakness in the lower limbs
  • decreased female reproductive ability
  • dehydration
  • drowsiness
  • nausea
  • vomiting
  • epigastric pain
  • hypertension
  • acute renal failure
  • hepatic failure
  • respiratory depression
  • coma
  • seizures
  • vascular collapse
  • cardiac arrest

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

Storage

This medication may be sensitive to light and should be stored in a container that does not allow light to enter. It is also advisable to store it at room temperature between 1 degree and 30 degrees Celsius. Proper storage helps maintain the efficacy of the medication for a longer period.

Appearance and packaging

Appearance

Light yellow powder contained in hard capsules that are light green in color.

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.