NO-SPA Max,80 mg, coated tablets
Drotaverine hydrochloride
{logo}
This medicine should always be taken exactly as described in the package leaflet or as directed by a doctor, pharmacist, or nurse.
No-Spa Max is a spasmolytic medicine that reduces pain (painful spasms) in the abdominal and pelvic cavities, i.e., in the digestive tract (stomach and intestines), bile ducts, and urinary tract, as well as in the female reproductive system.
No-Spa Max contains drotaverine hydrochloride as the active substance. This substance is used for smooth muscle spasms of both nervous and muscular origin, most often manifested by abdominal pain. The spasmolytic effect of drotaverine does not depend on the type of innervation and the location of the smooth muscles (digestive tract, urinary system, circulatory system, and bile ducts).
The medicine is metabolized in the liver and excreted mainly in the urine and to a lesser extent through the digestive tract.
and as an adjunct:
Before taking No-Spa Max, the patient should discuss it with their doctor or pharmacist.
Caution should be exercised when taking the medicine:
The patient should inform their doctor or pharmacist about all medicines they are currently taking or have recently taken, as well as any medicines they plan to take.
Caution should be exercised when taking No-Spa Max with levodopa (a medicine used for Parkinson's disease) due to reduced antiparkinsonian effect and increased tremors and stiffness.
The medicine can be taken with or without food.
If the patient is pregnant or breastfeeding, thinks they may be pregnant, or plans to have a child, they should consult their doctor or pharmacist before taking this medicine.
Drotaverine crosses the placenta.
The medicine should not be taken during labor.
It is not recommended to take this medicine during breastfeeding.
In therapeutic doses, No-Spa Max does not affect the ability to drive or operate machinery.
If dizziness occurs, the patient should avoid potentially hazardous activities, such as driving or operating machinery.
Each tablet contains 104 mg of lactose monohydrate, 1.04 mg of quinoline yellow lake (E 104), and 0.294 mg of soy lecithin. If the patient has previously been diagnosed with intolerance to some sugars, they should consult their doctor before taking the medicine. Due to the presence of quinoline yellow, the medicine may cause allergic reactions.
The medicine contains lactose monohydrate. If the patient has been diagnosed with intolerance to some sugars, they should consult their doctor before taking the medicine.
The medicine contains less than 1 mmol (23 mg) of sodium per dose, which means it is considered "sodium-free".
This medicine should always be taken exactly as described in the package leaflet or as directed by a doctor, pharmacist, or nurse. If in doubt, the patient should consult their doctor, pharmacist, or nurse.
Recommended dose
Use in children:
Clinical trials have not been conducted in children. Caution should be exercised when taking No-Spa Max in children over 12 years of age.
If it is necessary to use the medicinal product No-Spa Max in children over 12 years of age:
Without consulting a doctor, the medicine can be taken for a maximum of 7 days.
The dividing line on the tablet is not intended for dividing the tablet into two equal doses.
In case of taking a higher dose of the medicine than recommended, the patient should immediately consult their doctor or pharmacist.
In case of missing a dose, the patient should take it as soon as possible, unless it is almost time for the next dose.
The patient should not take a double dose to make up for the missed dose.
If the patient has any further doubts about taking the medicine, they should consult their doctor, pharmacist, or nurse.
Like all medicines, No-Spa Max can cause side effects, although not everybody gets them.
Rare(affect 1 to 10 in 10,000 patients):
Frequency not known(cannot be estimated from the available data):
If the patient experiences any side effects, including any possible side effects not listed in the leaflet, they should inform their doctor or pharmacist. Side effects can be reported directly to the Department of Post-Marketing Surveillance 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 gather more information on the safety of the medicine.
The medicine should be stored out of sight and reach of children.
Store in a temperature below 25°C. Store in the original packaging to protect from light.
Do not take the 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. The patient should ask their pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
The pack contains 10, 20, 24, 40, 48, 50, or 60 coated tablets.
The coated tablets are yellow, oblong, and biconvex. One side of the tablet has the inscription "NOSPA", and the other side has a dividing line that is not intended for dividing the tablet into two equal doses.
The coated tablets are packaged in blisters of PA/Al/PVC/Al or PVC/Al foil in a cardboard box.
Marketing authorization holder
Opella Healthcare Commercial Ltd.
Váci út 133. "E" épület 3. Emelet,
Manufacturer
Opella Healthcare Poland Sp. z o. o.
Rzeszów Branch
ul. Lubelska 52
35-233 Rzeszów
To obtain more detailed information, the patient should 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
Date of last revision of the leaflet:
Need help understanding this medicine or your symptoms? Online doctors can answer your questions and offer guidance.