Dolma Injection (Tramadol Hydrochloride)

Adult administration

Administer Tramadol Hydrochloride as an intravenous or intramuscular injection of 50-100mg at a time. Repeat injection may be administered every 4-5 hours as needed. The maximum daily dosage can be up to 400mg.

This medication may cause seizures if the recommended dosage is exceeded, so it is essential to adhere to the prescribed dosage. Patients with epilepsy or a risk of seizures should use this medication only when necessary. Prolonged use of this drug may lead to psychological and physical dependence, so patients at risk of drug abuse must be strictly monitored for a short duration. Caution is required when taken with alcohol or central nervous system depressants, as dangerous side effects such as severe sedation or respiratory depression may occur. Individuals who metabolize this medication rapidly due to genetic factors may have a higher risk of respiratory depression, requiring dose adjustments and symptom monitoring. This medication should not be used in children under 12 years old or in adolescents under 18 years old who have undergone specific surgeries, as there is a high risk of respiratory depression. When using injections, handle the container cautiously to prevent glass particle contamination, particularly with children and the elderly. This medication should not be administered to certain patients, including those with acute alcohol intoxication, central nervous system drug overdose, severe respiratory depression, head trauma, or brain lesions. Patients with severely impaired liver or kidney function, pregnant or nursing women, and those with specific allergies should avoid this medication. Concurrent use of this medication with others may increase the risk of side effects due to interactions, so it is crucial to consult a physician or pharmacist before use. Drowsiness and dizziness may occur during treatment, so avoid driving or operating dangerous machinery. During treatment, monitor carefully for abnormal symptoms such as seizures, respiratory depression, or hypersensitivity reactions, and inform medical professionals immediately if any unusual symptoms arise. In the case of overdose, severe respiratory depression and seizures may occur, requiring emergency treatment, with naloxone as a possible antidote. This medication may have restrictions or require caution based on specific age groups and conditions such as children, adolescents, the elderly, pregnant and nursing women; thus, it is essential to take it under the guidance of a professional.

Serious side effects

• Hives
• angioedema
• anaphylaxis
• severe allergic reactions
• respiratory depression
• difficulty breathing
• dyspnea
• asthma attacks
• severe skin reactions
• Stevens-Johnson syndrome

Mild side effects

• Drowsiness
• dizziness
• fatigue
• lethargy
• nausea
• vomiting
• headache
• feeling of heaviness in the head
• agitation
• tremors

Store this medication in a sealed container to protect it from air exposure, at room temperature between 1°C and 30°C. This will help maintain the drug's effectiveness and prevent degradation.

Appearance

Injection containing a colorless liquid in a brown ampoule

Package unit

1ml×50 ampoules