about the product

Lyophilizate for preparation of solution for intramuscular injection and solution for inhalation.
A porous mass or amorphous powder of white or white with a yellowish tinge of color.
1.16 mg or 5.80 mg of the active substance in ampoules of colorless medical glass of the 1st hydrolytic class or in vials of colorless glass of the 1st hydrolytic class, hermetically sealed with bromo-butyl rubber stoppers, compressed with combined caps.
1, 2, 3, 4 or 5 ampoules are placed in an uncoated contour cell package made of polyvinyl chloride film.

Original product

This product is a fully original Promomed product

On every original product you will see our brand label

Specifications

Name
AMBERWIN® Pulmo
Dosage form
LYOPHILIZATE FOR PREPARATION OF SOLUTION FOR INTRAMUSCULAR INJECTION AND SOLUTION FOR INHALATION
Nosological classification
Other drugs for the treatment of diseases of the respiratory system
INN
Tyrosyl-d-alanyl-glycyl-phenylalanyl-leucyl-arginine succinate
Dosages
1.16 mg; 5.8 mg
ATC code
R07AX
Active substance
Tyrosyl-D-alanyl-glycyl-phenylalanyl-leucyl-arginine succinate
Pharmacotherapeutic group
General therapy drugs

use

Always use the drug in full accordance with the recommendations of your doctor. If in doubt, consult your doctor.
Recommended dose:
Intramuscular injection
Intramuscularly, AMBERWIN® Pulmo is administered at a dose of 1.16 mg (1 ampoule or 1 vial of 1.16 mg) once a day.
Inhalation use
Inhaled, AMBERWIN® Pulmo is administered at a dose of 11.6 mg once a day (2 ampoules or 2 vials of 5.8 mg) using a nebulizer until the reservoir is completely empty (the duration of inhalation is 10-40 minutes).
Use in children and adolescents
The safety and efficacy of AMBERWIN® Pulmo in children aged 0 to 18 years have not been established. There is no data available.
Route and (or) method of administration
Community-acquired pneumonia
By inhalation.
A new coronavirus infection of moderate severity
Intramuscularly; by inhalation.
Duration of therapy
The duration of the course of treatment is 10 days.

Help

Package leaflet

The drug AMBERWIN® Pulmo contains the active ingredient tyrosyl-D-alanyl-glycyl phenylalanyl-leucyl-arginine succinate, which belongs to the group of drugs for the treatment of diseases of the respiratory system.

The drug AMBERWIN® Pulmo is used in adults over the age of 18 for:
• treatment of community-acquired pneumonia (pneumonia that occurs outside a medical facility or in the first 48 hours after hospitalization), as part of complex therapy;
• treatment of a new coronavirus infection of moderate severity, as part of complex therapy of viral lung damage.

Overdose symptoms
In case of overdose, the risk of lowering blood pressure, dizziness, and visual disturbances increases.
Overdose Treatment
In case of overdose, you will be treated depending on the clinical manifestations.

Like all medications, AMBERWIN® Pulmo can cause undesirable reactions, but they do not occur in everyone.
Possible adverse reactions that may occur when using AMBERWIN® Pulmo:
Rarely (may occur in no more than 1 person out of 1000):
• allergic reactions
• dizziness
• visual perception disorders
• lowering blood pressure
Is unknown (based on the available data, the frequency of occurrence cannot be estimated):
• burning sensation
• taste distortion (dysgeusia)
• cough
• an increase in the level of "liver" enzymes (alanine aminotransferase (ALT), aspartate aminotransferase (AST)) is determined by the results of a blood test.

Do not use AMBERWIN® Pulmo:
• if you are allergic to tyrosyl-D-alanyl-glycyl-phenylalanyl-leucyl-arginine succinate;
• if you are pregnant;
• If you are breastfeeding.

Tell your doctor that you are using, have recently used, or may start using any other medications.
The drug AMBERWIN® Pulmo enhances the effect of analgesic drugs. Naloxone (a drug that blocks the action of opioids) blocks the effects of AMBERWIN® Pulmo.

The holder of the registration certificate
Russian Federation
PROMOMED RUS LLC
Address: 13 Mira Avenue, building 1, office 13, Moscow, 129090
Phone: +7 (495) 640 25 28
Email: reception@promomed.pro
Manufacturer
Russian Federation
JSC "Biochemist"
Address: 15A Vasenko St., Saransk, 430030, Republic of Mordovia
Reporting of adverse reactions
Russian Federation
Federal Service for Healthcare Supervision
Address: 109012, Moscow, Slavyanskaya square, 4, building 1
Phone number: +7 800 550 99 03
Email: pharm@roszdravnadzor.gov.ru or npr@roszdravnadzor.gov.ru
Website: www.roszdravnadzor.gov.ru

Do not give the drug to children from 0 to 18 years of age, since the effectiveness and safety of using the drug in this age group has not been established.

During treatment with AMBERWIN® Pulmo, due to possible side effects (decreased blood pressure, which can lead to dizziness and impaired visual perception), be careful when performing potentially dangerous activities that require increased concentration and speed of psychomotor reactions (driving vehicles, working with moving mechanisms, dispatcher, operator)..

Keep the medicine out of the reach of children.
Do not use the drug after the expiration date (shelf life) indicated on the carton after "Good before".
The expiration date is the last day of the given month.
Store at temperatures below 25 ° C. Store in the original packaging (pack).
Do not dispose of the drug in the sewer. Ask the pharmacy employee how to dispose (destroy) drugs that are no longer needed. These measures will help protect the environment.

If you are pregnant or breastfeeding, assume that you have become pregnant, or plan to
pregnancy, consult your doctor before using the drug.
Pregnancy
Do not use AMBERWIN® Pulmo during pregnancy.
Breastfeeding
Do not use AMBERWIN® Pulmo during breast-feeding.