Ropinirole Krka – Ropinirole uses, dose and side effects

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2 mg, 4 mg, and 8 mg prolonged-release tablets are
ropinirole

What Ropinirole Krka is and what it is used for

The active substance in Ropinirole Krka is ropinirole which belongs to a group of medicines called dopamine agonists. Dopamine agonists affect the brain in a similar way to a natural substance called dopamine.

Ropinirole Krka prolonged-release tablets are used to treat Parkinson’s disease.

People with Parkinson’s disease have low levels of dopamine in certain parts of the brain. Ropinirole acts similarly to natural dopamine, which is why it helps reduce the symptoms of Parkinson’s disease.

Ropinirole contained in Ropinirole Krka may also be approved for the treatment of other conditions not mentioned in this product information. Ask your doctor, pharmacist, or another healthcare professional if you have any further questions, and always follow their instructions.

What you need to know before you use Ropinirole Krka

Do not use Ropinirole Krka

  • if you are allergic to ropinirole or any of the other ingredients of this medicine (listed in section 6).
  • if you have severe kidney disease.
  • if you have liver disease.

Tell your doctor if you think any of the above apply to you.

Warnings and cautions

Talk to your doctor or pharmacist before taking Ropinirole Krka:

  • if you are pregnant or think you may be pregnant
  • if you are breast-feeding
  • if you are younger than 18 years
  • if you have severe heart problems
  • if you have severe mental health problems
  • if you have had any unusual cravings and/or behaviors (see section 4)
  • if you do not tolerate certain sugars (such as lactose )

Tell your doctor if you think any of the above apply to you. Your doctor may decide that Ropinirole Krka is not suitable for you or that you need extra checks while you are taking it.

Tell your doctor if you or your family/caregiver notice that you develop a strong desire or desire to behave in ways that are unusual for you, or if you can not resist the impulse, drive, or temptation to perform certain activities. which may harm you or others. These behaviors are called impaired impulse control and can include gambling addiction, compulsive eating, compulsive buying, an abnormally high sex drive, or an increase in sexual thoughts and feelings. Your doctor may need to adjust your dose or discontinue treatment.

Tell your doctor if you experience symptoms such as depression, apathy, anxiety, fatigue, sweating, or pain after you have stopped taking or reduced your ropinirole treatment (so-called withdrawal syndrome after treatment with a dopamine agonist or DAWS). If the problems persist for more than a few weeks, your doctor may need to adjust your treatment.

Tell your doctor if you or your family/caregiver notice that you develop periods of overactivity, elation, or irritability (symptoms of mania). These may occur together with, or without, symptoms of disturbed impulse control (see above). Your doctor may need to adjust your dose or discontinue treatment.

While taking Ropinirole Krka

Tell your doctor if you or your family notice that you develop any unusual behaviors (such as unusual gambling or increased sexual desire and/or behavior) while taking Ropinirole Krka. Your doctor may need to change your dose or stop treatment.

Smoking and Ropinirole Krka

Tell your doctor if you start or stop smoking while taking Ropinirole Krka. Your doctor may need to change dose one.

Other medicines and Ropinirole Krka

Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines, including medicines obtained without a prescription or over-the-counter medicines.

Remember to tell your doctor or pharmacist if you are starting to take a new medicine while taking Ropinirole Krka.

Some medicines may affect the effect of Ropinirole Krka, or make you more likely to get side effects. Ropinirole Krka may also affect the effectiveness of other medicines.

These medicines include:

  • fluvoxamine used for depression
  • drugs for other mental problems, such as sulpiride
  • HRT (hormone replacement therapy)
  • metoclopramide, which is used to treat nausea and heartburn
  • ciprofloxacin or enoxacin, which are antibiotics
  • other drugs for the treatment of Parkinson’s disease.

Talk to your doctor if you are taking or have recently taken any of the above medicines.

You will need to take additional blood tests if you are taking the following medicines with Ropinirole Krka:

  • vitamin K antagonists (used to reduce the formation of blood clots) such as warfarin.

Ropinirole Krka with food and drink

You can take Ropinirole Krka with or without food.

Pregnancy, breastfeeding, and fertility

Ropinirole Krka is not recommended for use if you are pregnant unless your doctor has determined that the benefit to you if you take Ropinirole Krka outweighs the risk to your unborn baby. Ropinirole Krka is not recommended for breastfeeding as it may affect milk production.

Tell your doctor immediately if you are pregnant, think you may be pregnant, or are planning to have a baby. Your doctor will also advise you if you are breastfeeding or planning to do so. Your doctor may advise you to stop taking Ropinirole Krka.

Driving and using machines

Ropinirole Krka can make you feel sleepy. The medicine can make you feel extremely sleepy and sometimes you can fall asleep very suddenly without any warning. Ropinirole can cause hallucinations (see, hear or feel things that are not there). Do not drive or use machines if you are affected.

If you get such problems: do not drive, do not use machines, and do not put yourself in any situation where drowsiness or falling asleep can put you (or others) at risk of serious injury or danger to life. Do not participate in any of these activities until the discomfort has resolved.

Talk to your doctor if this becomes a problem for you.

You are responsible for assessing whether you are fit to drive a motor vehicle or perform work that requires sharpened attention. One of the factors that can affect your ability in these respects is the use of drugs due to their effects and/or side effects.

Descriptions of these effects and side effects can be found in other sections. Read all the information in this leaflet for guidance. If you are not sure, talk to your doctor or pharmacist.

Ropinirole Krka contains lactose

If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicine.

How to use Ropinirole Krka

Always take this medicine exactly as your doctor or pharmacist has told you. Ask your doctor or pharmacist if you are unsure.

Use for children and adolescents

Do not give Ropinirole Krka to children. Ropinirole Krka is not normally prescribed for people under 18 years of age.

You can get Ropinirole Krka as the only treatment to treat the symptoms of Parkinson’s disease. It can also be given with another medicine called L-dopa (also called levodopa ). If you take L-dopa, you may experience involuntary movements ( dyskinesia ) when you start taking Ropinirole Krka. Tell your doctor if this happens as your doctor may need to adjust the doses of the medicine you are taking.

Ropinirole Krka prolonged-release tablets are designed to release drugs over 24 hours. If you have a disease that causes your medicine to pass through the body too quickly, for example in case of diarrhea, the tablets may not dissolve completely and may not work properly. You may see tablets in your stool. If this happens, contact your doctor as soon as possible.

How much Ropinirole Krka do you need to take?

It may take some time to find the dose of Ropinirole Krka that is most suitable for you.

The recommended starting dose of Ropinirole Krka prolonged-release tablets is 2 mg once daily for the first week. Your doctor may increase your dose to 4 mg of Ropinirole Krka prolonged-release tablet once a day from the second week of treatment. If you are very old, your doctor may increase your dose more slowly. The doctor can then adjust your dose until you get the dose that is best for you. Some people take up to 24 mg of Ropinirole Krka prolonged-release tablets every day. 

If you experience side effects at the beginning of your treatment that you can not accept, talk to your doctor. Your doctor may advise you to switch to a lower dose of ropinirole film-coated tablets (tablets with faster release ) that you should take three times a day.

Do not take more Ropinirole Krka than your doctor has recommended.

It may take a few weeks before you get the effect of Ropinirole Krka.

How to take your dose of Ropinirole Krka

Take Ropinirole Krka once daily, at the same time each day.

Swallow Ropinirole Krka prolonged-release tablets whole with a glass of water.

DO NOT break, chew or crush the prolonged-release tablets.  If you do, there is a risk of overdose because the drug will be absorbed into your body too quickly.

DO NOT break, chew or crush the prolonged-release tablets. If you do, there is a risk of overdose because the drug will be absorbed into your body too quickly.

If you switch from ropinirole tablets to a faster release

To determine your dose of Ropinirole Krka prolonged-release tablets, your doctor will prescribe the dose of ropinirole film-coated tablets (tablets with faster release ) that you have taken.

Take your ropinirole film-coated tablets (tablets with faster release ) as usual the day before you change. Then take your Ropinirole Krka prolonged-release tablets the next morning and do not take any more ropinirole film-coated tablets (tablets with faster release ).

If you use more Ropinirole Krka than you should 

Contact a doctor or pharmacist immediately. If possible, show them the packaging.

A person who has taken an overdose of Ropinirole Krka may experience any of the following symptoms: nausea, vomiting, dizziness (a rotating sensation), drowsiness, mental or physical fatigue, fainting, or hallucinations.

If you have ingested too much medicine or if, for example, a child has accidentally ingested the medicine, contact a doctor or hospital for risk assessment and advice.

If you forget to use Ropinirole Krka

Do not take extra prolonged-release tablets or double doses to compensate for a missed dose.

If you forget to take your dose of Ropinirole Krka for one or more days, ask your doctor for advice on how to start taking it again.

If you stop using Ropinirole Krka

Do not stop taking Ropinirole Krka without talking to your doctor.

Take Ropinirole Krka for as long as your doctor prescribes it for you. Do not stop unless your doctor tells you to. If you suddenly stop taking Ropinirole Krka, your symptoms of Parkinson’s disease can quickly get much worse.

If treatment is stopped abruptly, it could lead to the development of a medical condition called a neuroleptic malignant syndrome, which can pose a serious health risk. Symptoms include akinesia (decreased muscle movement), stiff muscles, fever, unstable blood pressure, tachycardia (increased heart rate ), confusion, and decreased level of consciousness (eg coma ).

If you need to stop taking Ropinirole Krka, your doctor will gradually reduce your dose.

If you have any further questions on the use of this product, ask your doctor or pharmacist.

Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.

The side effects of Ropinirole Krka are more likely to occur at the beginning of treatment and/or when the dose is increased. They are usually mild and may decrease after a period of use of the drug. If you are concerned about any side effects, talk to your doctor.

Very common side effects (may affect more than 1 user in 10)

  • fainting 
  • drowsiness
  • nausea

Common side effects (may affect up to 1 in 10 people)

  • fall asleep very suddenly without first feeling sleepy (sudden sleep attacks)
  • hallucinations (see things that do not exist)
  • vomiting
  • dizziness (rotating sensation)
  • heartburn 
  • abdominal pain
  • constipation
  • swollen legs, feet, or hands

Uncommon side effects (may affect up to 1 in 100 people)

  • dizziness and fainting especially when suddenly getting up (this is due to a drop in blood pressure)
  • low blood pressure ( hypotension )
  • feeling very tired during the day (extreme drowsiness)
  • mental side effects such as delirium (pronounced confusion), delusions (irrational ideas), or paranoia (morbid suspicion)

Some patients may experience the following side effects ( no known frequency: cannot be calculated from the available data)

  • allergic reactions such as red, itchy swelling of the skin ( hives ). Swelling of the face, lips, mouth, tongue, or throat which may cause difficulty in swallowing or breathing as well as rash or intense itching (see section 2).
  • changes in liver function, which have been shown in blood tests.
  • act aggressively
  • excessive use of the drug (request for a higher dose of dopaminergic drugs than required to control motor problems, known as dopaminergic dysregulation syndrome)
  • inability to resist impulses urges, or temptations to perform actions that may be harmful to you or others, which may include:
    • a strong impulse to excessive gambling despite serious consequences for you personally or your family
    • changed or increased sexual interest or behavior that makes you or others noticeably worried, such as increased sexual drive
    • uncontrollable and excessive need to buy things and spend money
    • binge eating (eating large amounts of food in a short time) or compulsive eating (eating more food than normal and more than is needed to satisfy your hunger)
  • Depression, lethargy, anxiety, fatigue, sweating, or pain may occur after you stop taking or reduce your treatment with Ropinirole Krka (known as withdrawal syndrome after treatment with dopamine agonist or DAWS).
  • periods of overactivity, elation, or irritability

Tell your doctor if you experience any of these behaviors to discuss ways to manage or reduce the symptoms.

If you are taking Ropinirole Krka at the same time as L-dopa

People taking Ropinirole Krka at the same time as L-dopa may experience other side effects after a while:

  • Involuntary movements ( dyskinesias ) are a very common side effect of you taking L-dopa, you may experience involuntary movements ( dyskinesias ) when you start taking Ropinirole Krka. Tell your doctor if this happens as your doctor may need to adjust the dose of one of the medicines you are taking.
  • Confusion is a common side effect

How to store Ropinirole Krka

Keep this medicine out of the sight and reach of children.

Do not use this medicine after the expiry date which is stated on the blister and carton after EXP. The expiration date is the last day of the specified month.

Do not store above 30 ° C.

Store in the original package. Moisture sensitive.

Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment.

Contents of the packaging and other information

Content declaration

The active substance is ropinirole.

Ropinirole Krka 2 mg prolonged-release tablets:

Each prolonged-release tablet contains 2 mg ropinirole (as hydrochloride).

Ropinirole Krka 4 mg prolonged-release tablets:

Each prolonged-release tablet contains 4 mg of ropinirole (as hydrochloride).

Ropinirole Krka 8 mg prolonged-release tablets:

Each prolonged-release tablet contains 8 mg of ropinirole (as hydrochloride).

Other ingredients are:

Ropinirole Krka 2 mg prolonged-release tablets:

Hypromellose (type 2208), lactose monohydrate, anhydrous colloidal silica, carbomers 4000-11000 mPa.s, hydrogenated castor oil, magnesium stearate in the tablet core, and hypromellose (type 2910), titanium dioxide (E171), macrogol 400, red iron oxide (E172), yellow iron (E172) E172) in the film coating. See section 2 “Ropinirole Krka contains lactose”.

Ropinirole Krka 4 mg and 8 mg prolonged-release tablets:

Hypromellose (type 2208), lactose monohydrate, anhydrous colloidal silica, carbomers 4000-11000 mPa.s, hydrogenated castor oil, magnesium stearate in the tablet core, and hypromellose (type 2910), titanium dioxide (E171), macrogol 400, red iron oxide (E172), yellow iron (E172) E172), black iron oxide (E172) in the film coating. See section 2 “Ropinirole Krka contains lactose”.

What the medicine looks like and the contents of the pack

Ropinirole Krka 2 mg prolonged-release tablets:

The tablets are light red, biconvex, and oval.

Ropinirole Krka 4 mg prolonged-release tablets:

The tablets are light brown, biconvex, and oval.

Ropinirole Krka 8 mg prolonged-release tablets:

The tablets are brownish red, biconvex, and oval.

The tablets are supplied in cartons of 10, 21, 28, 30, 42, 60, 84 and 90 prolonged-release tablets in blisters (OPA / Al / PVC // Al).

Not all pack sizes may be marketed.

Marketing Authorization Holder and Manufacturer

Manufacturer

KRKA, dd, Novo mesto, Šmarješka cesta 6, 8501 Novo mesto, Slovenia

TAD Pharma GmbH, Heinz-Lohmann-Str. 5, 27472 Cuxhaven, Germany

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