Medication info

Dibeta C Injection (Diclofenac β-Dimethylaminoethanol)

Prescription medicationSolution주사
Ingredient · strength
Diclofenac Beta-Dimethylaminoethanol›45mg / 1mL
Manufacturer / importer
대화제약(주)
Appearance
A brown ampoule containing a colorless to pale yellow transparent solution
Packaging
2ml/ampoule x 50
Approval status
Active

MFDS item code 200002445 · Notified 2000.11.15 · Insurance code 645600641

Summary

Main use
Pain relief for rheumatoid arthritis, osteoarthritis, etc. (arthritis)
Who receives it
Adults
Adult administration
As Diclofenac β-Dimethylaminoethanol, administer 90mg intramuscularly deeply in the upper outer quadrant of one buttock daily. In severe cases, it can be administered as 90mg twice a day, alternating injections in both buttocks. After the initial treatment period, tablets or suppositories should be switched for administration. Adjust doses appropriately based on age, disease, and symptoms. To minimize cardiovascular adverse reactions, use the lowest effective dose for the shortest duration.

Ingredients

Manufacturer
대화제약(주)

Efficacy & effects

Pain relief for rheumatoid arthritis, osteoarthritis, etc. (arthritis)

  • Rheumatoid arthritis
  • osteoarthritis
  • ankylosing spondylitis
  • post-traumatic inflammation
  • post-surgical inflammation
  • pain
  • acute gout
  • renal colic
  • hepatic colic
View approved original text

This medication is used for major arthritis diseases such as rheumatoid arthritis, osteoarthritis, and ankylosing spondylitis. It also helps relieve inflammation and pain that occurs after trauma or surgery, acute gout, and renal or hepatic colic. This drug is effective in improving various inflammatory diseases and pain.

How it is given

Adult administration

As Diclofenac β-Dimethylaminoethanol, administer 90mg intramuscularly deeply in the upper outer quadrant of one buttock daily. In severe cases, it can be administered as 90mg twice a day, alternating injections in both buttocks. After the initial treatment period, tablets or suppositories should be switched for administration. Adjust doses appropriately based on age, disease, and symptoms. To minimize cardiovascular adverse reactions, use the lowest effective dose for the shortest duration.

Precautions

Patients who consume more than three alcoholic beverages regularly each day should consult with a doctor or pharmacist before taking this medication. This medication may cause gastrointestinal bleeding, which requires special caution. Individuals with cardiovascular issues or risk factors should be closely monitored as serious cardiovascular problems such as myocardial infarction or stroke may occur while taking this medication. This medication can cause serious gastrointestinal side effects such as bleeding, ulcers, or perforation, with elderly individuals at higher risk. Immediate treatment is required if symptoms of gastrointestinal bleeding or ulcers occur, and medication should be discontinued if necessary. Allergic reactions may cause severe chest pain or myocardial infarction; thus, if chest pain occurs, medical personnel should be notified immediately. Ampoule injections may contain glass fragments, so care should be taken during use, especially for children and the elderly. Products containing benzyl alcohol may cause fatal respiratory problems in premature infants, so caution is warranted. Patients with a history of peptic ulcers, severe blood disorders, severely impaired hepatic or renal function, severe hypertension, or heart failure, as well as those allergic to any component of this drug, should not take it. Individuals allergic to aspirin or other non-steroidal anti-inflammatory drugs should also refrain from using this medication. Young newborns, premature infants, and patients with cardiovascular diseases should avoid this medication. Individuals with a history of peptic ulcers, blood disorders, impaired hepatic or renal function, hypertension, heart failure, asthma, ulcerative colitis, Crohn's disease, the elderly, and children should use this medication cautiously. Special care should be taken in cases where sodium metabisulfite is present, as it may cause allergic reactions. Rarely, this medication may cause shock, gastrointestinal bleeding, blood disorders, severe skin reactions, hepatic and renal dysfunction, hypersensitivity, and neurologic symptoms; if any adverse symptoms occur, consultation with medical personnel is necessary. Regular blood tests and liver and kidney function tests are required during prolonged use, and medication should be stopped if abnormal signs are detected. This medication may worsen hypertension and cause fluid retention and edema; therefore, individuals with hypertension or heart failure should exercise particular caution. During pregnancy, especially in the late stage, it may have serious effects on the fetus, so pregnant women should avoid use, and breastfeeding mothers should consult before taking it as adverse reactions may occur in the baby. This medication may interact with other non-steroidal anti-inflammatory drugs, aspirin, anticoagulants, lithium, methotrexate, etc., so caution should be taken when used in combination, and consultation with medical personnel is required. Elderly individuals and children should be administered the minimum dose with special attention to adverse reactions.

Side effects and when to seek care immediately

Serious side effects

  • Hives
  • swelling
  • chest tightness
  • difficulty breathing
  • shock
  • cardiovascular thrombotic reactions
  • myocardial infarction
  • stroke
  • gastrointestinal bleeding
  • ulcers
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  • perforation
  • Stevens-Johnson syndrome
  • Lyell's syndrome
  • photosensitivity
  • jaundice
  • liver dysfunction
  • acute renal failure
  • oliguria
  • hematuria
  • asthma attacks
  • rash
  • decreased blood pressure
  • Kounis syndrome
  • severe allergic reactions
  • severe skin reactions
  • respiratory issues
  • liver abnormalities
  • severe neurological symptoms
  • edema
  • urination difficulties

Mild side effects

  • Loss of appetite
  • nausea
  • vomiting
  • abdominal pain
  • diarrhea
  • stomatitis
  • thirst
  • constipation
  • headache
  • drowsiness
Show 16 more
  • dizziness
  • insomnia
  • nervousness
  • numbness
  • confusion
  • hallucinations
  • seizures
  • visual disturbances
  • tinnitus
  • increased blood pressure
  • decreased blood pressure
  • palpitations
  • tachycardia
  • general fatigue
  • sweating
  • hair loss

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

Storage

This medication should be stored in a tightly sealed container that blocks light, and it is important to keep it at a temperature between 1 and 30 degrees Celsius. Storing it this way preserves the medication's effectiveness and prevents degradation.

Appearance and packaging

Appearance

A brown ampoule containing a colorless to pale yellow transparent solution

Package unit

2ml/ampoule x 50

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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For anything that needs medical judgment, consult a doctor or pharmacist.

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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.