Panadol Femina 10 tablets
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Product name: Panadol Femina 10 tablets
The drug contains two drugs, paracetamol - analgesic (painkiller) and butylscopolamine bromide - antispasmodic (anticonvulsant).
Application:
- treatment of symptoms of dysmenorrhoea or other visceral pains
- during radiodiagnostic procedures and before gastrointestinal endoscopy
Dosage and dosage schedules
Adults and children over 12 years of age
- with a body weight of 34-60 kg: take 1 tablet 1-3 times a day. The interval between doses should be at least 8 hours.
- with a body weight over 60 kg: take 2 tablets 1-3 times a day. The interval between doses should be at least 8 hours.
The maximum daily dose is 6 tablets. Do not exceed the recommended dosage.
Without consulting a doctor, the drug can be taken for no longer than 3 days.
Method of use
The tablet should be swallowed whole with plenty of liquid. The effect of food on the rate and intensity of the effect is not reported.
Notice
The drug may be taken during pregnancy only on the advice of a doctor and after weighing the risks and benefits of treatment.
The drug is contraindicated during breastfeeding.
The drug is not suitable for children under 12 years of age.
Increased caution is needed in patients with renal and hepatic impairment and in patients with heart disease (mitral stenosis, coronary artery disease).
Alcohol should not be consumed during treatment (risk of hepatotoxicity).
During treatment, other drugs containing paracetamol should not be taken concomitantly.
The drug can aggravate gastroesophageal reflux, peristalsis of the upper gastrointestinal tract, pyloric stenosis.
The drug can cause dry mouth, constipation and, especially in men, urinary retention.
The drug may increase intraocular pressure, if visual acuity impairment or pain in the eyeball occurs, treatment should be discontinued and it is necessary to see a doctor.
The drug can affect the central nervous system and provoke impaired accommodation, during treatment, driving and working with machines is prohibited.
The drug contains sorbitol.
further special warnings are given in the SPC (section 4.4).
paracetamol, butylscopolamine bromide
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