Gripex Control,500 mg + 50 mg, tablets
Paracetamol + Caffeine
This medicine should always be taken exactly as described in the patient leaflet or as directed by a doctor or pharmacist.
The indications for use of this medicine are: muscle, joint, and bone pain of various origins, headaches, migraines, neuralgia, sore throat, toothache, and menstrual pain, post-traumatic, post-operative, and tumor pain of mild or moderate intensity, feverish conditions resulting from colds, flu, and flu-like conditions.
If after 3 days there is no improvement or you feel worse, consult a doctor.
Before taking Gripex Control, discuss it with your doctor or pharmacist.
used to treat cold and flu symptoms) due to the risk of overdose, which can lead to life-threatening liver damage.
While taking Gripex Control, immediately inform your doctor if you have severe illnesses, including severe kidney dysfunction or sepsis (when bacteria and their toxins are present in the blood, leading to organ damage) or malnutrition, chronic alcoholism, or if you are also taking flucloxacillin (an antibiotic). In these situations, patients have been reported to develop a severe disease called metabolic acidosis (abnormality of blood and body fluids), when they took paracetamol in regular doses for a longer period or when they took paracetamol with flucloxacillin. Symptoms of metabolic acidosis may include: severe breathing difficulties, including rapid deep breathing, drowsiness, feeling of nausea (nausea) and vomiting.
The medicine should not be taken by children under 12 years of age.
Tell your doctor or pharmacist about all medicines you are taking, have recently taken, or plan to take.
Do not take Gripex Control with other medicines containing paracetamol and caffeine.
In case of concurrent use of oral antidiabetic drugs, anticoagulants (warfarin, coumarin), rifampicin (a drug used to treat tuberculosis), antiepileptic drugs, sedatives and hypnotics, MAO inhibitors (drugs used, among others, in depression), zidovudine (an antiviral drug used in HIV infection), sympathomimetic drugs (i.e., decongestants, appetite suppressants, and psychostimulants similar to amphetamine), thyroid hormones, oral contraceptives, cimetidine (a drug used mainly in gastric and duodenal ulcer disease), chloramphenicol (an antibiotic), quinolones (bactericidal drugs), and verapamil (a drug used in heart disease) - consult your doctor before taking Gripex Control.
Tell your doctor or pharmacist if you are taking flucloxacillin (an antibiotic), due to the serious risk of blood and body fluid disorders (called metabolic acidosis), which must be treated urgently (see section 2).
See section 3.
Do not drink alcohol while taking the medicine, due to the increased risk of liver damage.
If you are pregnant or breastfeeding, think you may be pregnant, or plan to have a child, consult your doctor or pharmacist before taking this medicine.
Do not take in the first trimester of pregnancy. In the second and third trimesters, consult your doctor before taking the medicine.
Do not take during breastfeeding.
It does not affect the ability to drive and use machines.
The medicine contains less than 1 mmol (23 mg) of sodium per single dose (2 tablets), which means the medicine is considered "sodium-free".
This medicine should always be taken exactly as described in the patient leaflet or as directed by a doctor or pharmacist. If you have any doubts, consult your doctor or pharmacist.
Orally, 1 or 2 tablets every 4 to 6 hours (maximum 8 tablets per day).
Do not give to children under 12 years of age.
It is recommended to take the medicine on an empty stomach, as this allows for faster pain-relieving and antipyretic effects.
The dividing line on the tablet is only to facilitate breaking it, for easier swallowing, and not for dividing into equal doses.
If you have taken a higher dose of the medicine than recommended, contact your doctor immediately, even if you feel well. If the overdose occurred no more than 1 hour ago, induce vomiting. Contact your doctor immediately, as specialized treatment in a hospital setting may be necessary.
Symptoms may include: severe nausea, vomiting, excessive sweating, drowsiness, general weakness, abdominal pain, increased urination, dehydration, and fever. More severe poisoning is characterized by cardiac arrhythmia and tonic-clonic seizures. Some symptoms may resolve the next day, despite the fact that life-threatening liver damage is developing, which will then manifest as abdominal distension, return of nausea, and jaundice.
Do not take a double dose to make up for a missed dose.
If you have any further doubts about taking this medicine, consult your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
They include:
If you experience any side effects, including any not listed in this leaflet, tell your doctor or pharmacist.
Side effects can be reported directly to the Department of Post-Marketing Surveillance of Medicinal Products, Medical Devices, and Biocidal Products
Jerozolimskie Avenue 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.
By reporting side effects, you can help provide more information on the safety of this medicine.
Store in a temperature below 30°C.
Keep the medicine out of sight and reach of children.
Do not take the medicine after the expiration date stated on the carton and blister pack (month/year).
The applied labeling for the blister is: EXP - expiration date, Lot - batch number.
The active substances of the medicine are:
paracetamol
500 mg
caffeine
50 mg.
The other ingredients are: povidone, microcrystalline cellulose, sodium carboxymethylcellulose (Type A),
silica colloidal anhydrous, magnesium stearate.
White, elongated tablets, convex on both sides, with a dividing line.
Packaged in blisters and a carton with a leaflet.
The medicine is available in packs of:
2, 4, 6, 8, 10, 12 tablets in blisters.
Not all pack sizes may be marketed.
US Pharmacia Sp. z o.o.
Ziębicka 40
50-507 Wrocław
To obtain more detailed information about this medicine, contact:
USP Zdrowie Sp. z o.o.
Poleczki 35
02-822 Warsaw
phone: +48 (22) 543 60 00
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