Drotaverine Hydrochloride
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No-Spa Ampoules is a solution for subcutaneous, intramuscular, and intravenous injection, containing the active substance drotaverine. Drotaverine belongs to the group of antispasmodic drugs. It is used in smooth muscle spasm of both nervous and muscular origin. The spasmolytic effect of drotaverine does not depend on the type of innervation and localization of smooth muscles (gastrointestinal tract, urogenital system, cardiovascular system, and bile ducts).
Before starting to use No-Spa Ampoules, discuss it with your doctor.
Caution should be exercised when administering No-Spa Ampoules:
The medicine contains sodium metabisulfite, which may cause severe hypersensitivity reactions, including anaphylactic symptoms and bronchospasm. This applies especially to sensitive patients, particularly those with asthma and allergy in their history. In case of hypersensitivity to sodium metabisulfite, avoid parenteral administration of the medicine.
Tell your doctor about all the medicines you are taking now or have recently taken, as well as any medicines you plan to take.
Phosphodiesterase inhibitors, such as papaverine (a smooth muscle relaxant of internal organs) and its derivatives, reduce the antiparkinsonian effect of levodopa (a medicine used in Parkinson's disease). When drotaverine and levodopa are used together, the patient may experience increased tremors and stiffness.
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor for advice before taking this medicine.
Drotaverine crosses the placenta.
Do not use the medicine during labor.
The use of this medicine is not recommended during breastfeeding.
After parenteral administration, especially intravenous, avoid potentially hazardous activities, such as driving or operating machinery.
The medicine may rarely cause severe hypersensitivity reactions and bronchospasm.
This medicine should always be used as directed by your doctor or pharmacist.
If you are unsure, ask your doctor or pharmacist.
The medicine is for subcutaneous, intramuscular, or intravenous use.
The daily dose is 40 to 240 mg and should be administered in 1 to 3 divided doses, subcutaneously or intramuscularly.
In case of acute bile duct or kidney colic, 40 to 80 mg of drotaverine is administered slowly (approx. 30 seconds) intravenously.
In other spastic abdominal pains, 40 to 80 mg of drotaverine is administered intramuscularly or subcutaneously. If necessary, the dose of the medicine can be repeated up to 3 times a day.
If you feel that the effect of No-Spa Ampoules is too strong or too weak, ask your doctor.
In case of overdose, contact your doctor immediately.
If you miss a dose, take it as soon as possible, unless it is close to the time of the next dose.
Do not take a double dose to make up for a missed dose.
If you have any further questions about using this medicine, ask your doctor.
Like all medicines, No-Spa Ampoules can cause side effects, although not everybody gets them.
Side effects during treatment with drotaverine are rare.
Rare(may affect up to 1 in 1000 people):
Frequency not known(cannot be estimated from the available data):
In patients treated with drotaverine in the form of a solution for injection, anaphylactic shock may occur, with an unknown frequency, which can lead to death.
If you experience any side effects, including any not listed in this leaflet, please tell your doctor, pharmacist, or nurse. Side effects can be reported directly to the Department of Monitoring of Adverse Reactions to Medicinal Products of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products
Al. Jerozolimskie 181C
02-222 Warsaw
Phone: +48 22 49 21 301
Fax: +48 22 49 21 309
website: https://smz.ezdrowie.gov.pl
Side effects can also be reported to the marketing authorization holder or its representative in Poland.
Reporting side effects will help to gather more information on the safety of this medicine.
Keep the medicine out of the sight and reach of children.
Store the medicine at a temperature below 25°C. Protect from light.
Do not use this medicine after the expiry date stated on the packaging. The expiry date refers to the last day of the month.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
The pack contains 5 or 25 ampoules of orange glass, 2 ml each, in a cardboard box.
Marketing authorization holder
Opella Healthcare Commercial Ltd.
Váci út 133. „E” épület 3. Emelet,
Manufacturer
CHINOIN Pharmaceutical and Chemical Works Private Co. Ltd.
3510 Miskolc
Csanyikovölgy
Hungary
To obtain more detailed information, please contact the representative of the marketing authorization holder:
Opella Healthcare Poland Sp. z o.o.
ul. Marcina Kasprzaka 6
01-211 Warsaw
Phone: +48 22 280 00 00
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