Viprosal B® (Ointment) Instructions for Use
ATC Code
M02AX10 (Other drugs)
Clinical-Pharmacological Group
Drug with local irritant and analgesic action
Pharmacotherapeutic Group
Drugs for external use for muscle and joint pain; other drugs for external use for muscle and joint pain
Pharmacological Action
A drug for external use containing viper venom. It has a local irritant and analgesic effect.
It irritates the sensitive receptors of the skin and subcutaneous tissue, dilates blood vessels, and improves tissue trophism.
Indications
- Neuralgia;
- Arthralgia;
- Myositis.
ICD codes
| ICD-10 code | Indication |
| M25.5 | Pain in joint |
| M60 | Myositis |
| M79.1 | Myalgia |
| M79.2 | Neuralgia and neuritis, unspecified |
| ICD-11 code | Indication |
| 8E4A.1 | Paraneoplastic or autoimmune diseases of the peripheral or autonomic nervous system |
| FB30 | Infectious myositis |
| FB32 | Other specified disorders of muscle |
| FB3Z | Disorder of muscle, unspecified |
| FB56 | Specified soft tissue diseases, not elsewhere classified |
| FB56.0 | Granuloma of soft tissue due to foreign body, not elsewhere classified |
| FB56.2 | Myalgia |
| ME82 | Pain in joint |
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. |
Ointment
For external use in adults and children over 12 years of age.
Depending on the size of the skin surface, apply small portions of 5-10 g (1-2 teaspoons) of the ointment to the painful area and rub into the skin 1-2 times/day depending on the intensity of the pain until the pain syndrome disappears.
The duration of the treatment course depends on the nature and severity of the disease.
The patient should consult a doctor if the symptoms of the disease persist after a 14-day course of treatment.
Adverse Reactions
Allergic reactions itching, swelling, or urticaria.
To avoid side effects, it is recommended to first apply a small amount of the ointment to the skin to determine sensitivity to the drug.
If side effects occur, the patient should consult a doctor.
Contraindications
- Hypersensitivity to the components of the drug.
- Skin lesions;
- Skin diseases (including those of allergic and bacterial origin);
- Febrile conditions;
- Pulmonary tuberculosis;
- Cerebral and coronary circulation disorders;
- Predisposition to angiospasms;
- Severe renal impairment;
- Severe hepatic impairment;
- General exhaustion;
- Children under 12 years of age;
- Pregnancy;
- Breastfeeding period.
Use in Pregnancy and Lactation
The drug is contraindicated for use during pregnancy and lactation (breastfeeding).
Use in Hepatic Impairment
The drug is contraindicated in severe hepatic impairment.
Use in Renal Impairment
The drug is contraindicated in severe renal impairment.
Pediatric Use
Contraindication: children under 12 years of age.
Special Precautions
If the ointment is accidentally swallowed, a doctor should be consulted.
The ointment must not be applied to damaged skin.
If accidentally applied to mucous membranes, the ointment causes severe irritation.
After applying the ointment, wash hands thoroughly to avoid getting the ointment into the eyes and on mucous membranes.
If the ointment gets into the eyes or on mucous membranes, rinse them abundantly with water.
Effect on the ability to drive vehicles and operate machinery
The use of the drug does not affect the ability to perform potentially hazardous activities requiring increased concentration and speed of psychomotor reactions (driving vehicles, working with moving machinery, work of a dispatcher and operator).
Overdose
To date, no cases of overdose with Viprosal B® have been reported.
Drug Interactions
Not described.
Storage Conditions
The drug should be stored out of the reach of children at a temperature not exceeding 25°C (77°F). Do not store in the refrigerator or freezer.
Shelf Life
The shelf life is 3 years.
Dispensing Status
The drug is available without a prescription.
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
Ointment for external use: tubes 30 g or 50 g
Marketing Authorization Holder
Grindeks, JSC (Latvia)
Dosage Form
| Viprosal B® | Ointment for external use: tubes 30 g or 50 g |
Dosage Form, Packaging, and Composition
Ointment for external use white or white with a slightly yellowish tint, with the smell of camphor or turpentine.
| 1 g | |
| Vipera berus venom dried | 0.05 MU* |
| Racemic camphor | 30 mg |
| Turpentine gum | 30 mg |
| Salicylic acid | 10 mg |
* MU – Mouse Units.
Excipients : petrolatum, cetearyl alcohol, hard paraffin, sodium cetylstearyl sulfate, glycerol, sodium chloride, purified water – up to 1 g.
30 g – aluminum tubes (1) – cardboard boxes.
50 g – aluminum tubes (1) – cardboard boxes.
Ointment for external use: tubes 30 g or 50 g
Marketing Authorization Holder
Grindeks, JSC (Latvia)
Dosage Form
| Viprosal B® | Ointment for external use: tubes 30 g or 50 g |
Dosage Form, Packaging, and Composition
Ointment for external use white or white with a slightly yellowish tint, with the smell of camphor or turpentine.
| 1 g | |
| Vipera berus venom dry | 0.05 MU* |
| Racemic camphor | 30 mg |
| Turpentine gum | 30 mg |
| Salicylic acid | 10 mg |
* MU – Mouse Units.
Excipients : petrolatum, cetearyl alcohol, hard paraffin, sodium cetylstearyl sulfate, glycerol, sodium chloride, purified water – up to 1 g.
30 g – aluminum tubes (1) – cardboard boxes.
50 g – aluminum tubes (1) – cardboard boxes.
Ointment for external use: 30 g, 50 g or 75 g tubes
Marketing Authorization Holder
Grindeks, JSC (Latvia)
Manufactured By
Tallinn Pharmaceutical Plant, JSC (Estonia)
Contact Information
GRINDEX JSC (Latvia)
Dosage Form
| Viprosal B® | Ointment for external use: 30 g, 50 g or 75 g tubes |
Dosage Form, Packaging, and Composition
Ointment for external use white or white with a slightly yellowish tint, with the smell of camphor or turpentine.
| 1 g | |
| Vipera berus venom dried | 0.05 MU |
| Racemic camphor | 30 mg |
| Turpentine gum | 30 mg |
| Salicylic acid | 10 mg |
Excipients : petrolatum, cetearyl alcohol, hard paraffin, sodium cetylstearyl sulfate, glycerol, sodium chloride, purified water – up to 1 g.
30 g – aluminum tubes (1) – cardboard boxes.
50 g – aluminum tubes (1) – cardboard boxes.
75 g – aluminum tubes (1) – cardboard boxes.
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