Ubistesin (Solution) Instructions for Use
ATC Code
N01BB58 (Articaine in combination with other drugs)
Active Substances
Articaine (Rec.INN registered by WHO)
Epinephrine (Rec.INN registered by WHO)
Clinical-Pharmacological Group
Local anesthetic with a vasoconstrictor component for use in dentistry
Pharmacotherapeutic Group
Local anesthetic agent + alpha- and beta-adrenomimetic
Pharmacological Action
A combined medicinal product that exerts a local anesthetic effect.
Articaine is a local anesthetic of the amide type from the thiophene series. Its mechanism of action is due to the stabilization of neuronal membranes and the prevention of the generation and conduction of nerve impulses.
Epinephrine is an adrenomimetic. It causes vasoconstriction at the site of injection, which impedes the absorption of articaine and prolongs the duration of the local anesthetic effect.
The onset of action is 0.5-3 minutes, and the duration of action is 45 minutes.
Indications
Infiltration and conduction anesthesia (including in dentistry – tooth extraction, cavity filling, tooth preparation for crowns).
ICD codes
| ICD-10 code | Indication |
| Z51.4 | Preparatory procedures for subsequent treatment or examination, not elsewhere classified |
| ICD-11 code | Indication |
| QB9A | Preparatory procedures for subsequent treatment |
Dosage Regimen
| The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen. |
Solution
Infiltration anesthesia: tonsillectomy (for each tonsil) – 5-10 ml; reduction of fractures – 5-20 ml; perineal suture – 5-15 ml.
Conduction anesthesia: Oberst’s anesthesia – 2-4 ml, retrobulbar – 1-2 ml, intercostal – 2-4 ml (per segment), paravertebral – 5-10 ml, peridural (epidural) – 10-30 ml, sacral – 10-30 ml, trigeminal nerve block – 1-5 ml, stellate ganglion block – 5-10 ml, brachial plexus block – 10-30 ml (supraclavicular or axillary approach), external genitalia block – 7-10 ml (per side), paracervical block – 6-10 ml (per side).
For uncomplicated extraction of maxillary teeth in a non-inflammatory stage, inject under the mucous membrane in the area of the transitional fold – vestibular depot 1.7 ml per tooth, if necessary – an additional 1-1.7 ml; palatal incision or suture – palatal depot 0.1 ml.
For extraction of mandibular premolars (5-5) in an uncomplicated stage, infiltration anesthesia provides the effect of conduction anesthesia.
For cavity preparation and tooth preparation for crowns, except for mandibular molars – vestibular injection of 0.5-1.7 ml per tooth. The maximum dose is 7 mg/kg.
Adverse Reactions
From the central nervous system (depends on the dose used): headache, impaired consciousness (up to loss of consciousness); respiratory disorders (up to apnea); tremor, muscle twitching, convulsions.
From the digestive system: nausea, vomiting, diarrhea.
From the sensory organs: rarely – transient visual disturbances (up to blindness), diplopia.
From the cardiovascular system: decreased blood pressure, tachycardia, bradycardia, arrhythmia.
Allergic reactions: skin hyperemia and itching, conjunctivitis, rhinitis, angioedema of varying severity (including edema of the upper and/or lower lip and/or cheeks, glottis with difficulty swallowing, urticaria, difficulty breathing), anaphylactic shock.
Local reactions: swelling or inflammation at the injection site, appearance of ischemic zones at the injection site (up to the development of tissue necrosis – in case of accidental intravascular injection); nerve damage (up to the development of paralysis) – occurs only if the injection technique is violated.
Contraindications
B12-deficiency anemia; methemoglobinemia; paroxysmal ventricular tachycardia; atrial tachyarrhythmia; closed-angle glaucoma; hypoxia; intolerance to sulfogroups (especially in bronchial asthma); hypersensitivity to the components of the combination.
With caution: cholinesterase deficiency, renal failure, bronchial asthma, diabetes mellitus, hyperthyroidism, arterial hypertension, children’s age (under 4 years – efficacy and safety have not been established).
For paracervical block: preeclampsia, bleeding in the third trimester of pregnancy, amnionitis.
Use in Pregnancy and Lactation
It does not have a harmful effect on the fetus (with the exception of possible bradycardia) with any technique of application and dosage.
During lactation, there is no need to interrupt breastfeeding, because clinically significant concentrations of articaine are not detected in breast milk.
Use in Renal Impairment
With caution: renal failure.
Pediatric Use
With caution: children’s age (under 4 years – efficacy and safety have not been established).
Special Precautions
Do not administer intravenously! To avoid intravascular injection, an aspiration test must be performed. The injection pressure should correspond to the sensitivity of the tissue.
Injection should not be performed into an inflamed area.
Food intake is possible only after sensitivity is restored.
Effect on the ability to drive vehicles and mechanisms
The patient’s admission to driving vehicles or engaging in activities requiring high mental and motor reactions is determined by the doctor.
Drug Interactions
Tricyclic antidepressants, MAO inhibitors enhance the hypertensive effect.
The local anesthetic effect of articaine is enhanced and prolonged by vasoconstrictors.
Non-selective beta-blockers increase the risk of hypertensive crisis and severe bradycardia.
Storage Conditions
Store at 2°C (36°F) to 25°C (77°F). Keep in original packaging, protected from light. Keep out of reach of children.
Dispensing Status
Rx Only
Important Safety Information
This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.
Medical DisclaimerBrand (or Active Substance), Marketing Authorisation Holder, Dosage Form
Solution for injection 40 mg+0.005 mg/1 ml: cartridges 1.7 ml 50 pcs.
Marketing Authorization Holder
3M Deutschland, GmbH (Germany)
Dosage Form
| Ubistesin | Solution for injection 40 mg+0.005 mg/1 ml: cartridges 1.7 ml 50 pcs. |
Dosage Form, Packaging, and Composition
Solution for injection transparent, colorless, without opalescence.
| 1 ml* | |
| Articaine hydrochloride | 40 mg |
| Epinephrine (as epinephrine hydrochloride) | 0.006 mg |
| Corresponding to epinephrine content | 0.005 mg |
Excipients: sodium sulfite (E221), sodium chloride, hydrochloric acid solution 14% (for pH adjustment), sodium hydroxide solution 9% (for pH adjustment), water for injection.
1.7 ml – cartridges made of colorless neutral glass (50) – tin cans with foam polyethylene pads.
* Each cartridge with 1.7 ml of solution for injection contains 68 mg of articaine hydrochloride and 0.0085 mg of epinephrine (as epinephrine hydrochloride).
Solution for injection 40 mg+0.01 mg/1 ml: cartridges 1.7 ml 50 pcs.
Marketing Authorization Holder
3M Deutschland, GmbH (Germany)
Dosage Form
| Ubistesin forte | Solution for injection 40 mg+0.01 mg/1 ml: cartridges 1.7 ml 50 pcs. |
Dosage Form, Packaging, and Composition
Solution for injection transparent, colorless, without opalescence.
| 1 ml* | |
| Articaine hydrochloride | 40 mg |
| Epinephrine (as epinephrine hydrochloride) | 0.012 mg |
| Corresponding to epinephrine content | 0.01 mg |
Excipients: sodium sulfite (E221), sodium chloride, hydrochloric acid solution 14% (for pH adjustment), sodium hydroxide solution 9% (for pH adjustment), water for injection.
1.7 ml – cartridges made of colorless neutral glass (50) – tin cans with foam polyethylene pads.
* Each cartridge with 1.7 ml of solution for injection contains 68 mg of articaine hydrochloride and 0.017 mg of epinephrine (as epinephrine hydrochloride).
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