Geffer Trattamento Iperacidità granulato 24 Bustine 5g

Therapeutic indications
Geffer Granulate is used in the symptomatic treatment of hyperacidity (pain and heartburn), when accompanied by slowing of gastric transit, nausea, aerophagia and meteorism.

Dosage and method of use
Geffer Granulate should be taken in the following doses and methods: 1 sachet in half a glass of water before meals or at the onset of disorders, 2-3 times a day. Do not exceed the recommended doses: in particular elderly patients should follow the minimum dosages indicated above. The use of the product is limited to adult patients

Contraindications

Hypersensitivity to any of the active substances or excipients.
Patients with glaucoma, pheochromocytoma, epileptic disease, Parkinson's disease and other conditions
overt extrapyramidal or in the course of therapy with anticholinergics.
Cases in which the stimulation of intestinal motility can be dangerous, for example in
presence of gastrointestinal bleeding, perforation, mechanical obstruction.
Patients with Porphyria.
Children under the age of 16.
Pregnancy and breastfeeding
Special warnings
Avoid the simultaneous administration of neuroleptics, phenothiazines, butyrophenones, thioxanthenes, etc., sedatives and alcohol. The use of the product can give rise to disturbances such as to alter the normal state of alertness; this should be taken into account by patients engaged in driving vehicles or operating with potentially dangerous machinery.

After a maximum of 3 days of treatment without appreciable results, consult your doctor. Elderly patients should not exceed 3 days of consecutive treatment e
must comply with the minimum dosages indicated. One sachet of Geffer contains 287 mg (12.5 mmol) of sodium: this should be taken into account in case of hypertension and in all situations requiring a controlled sodium intake (patients with congestive heart failure, renal insufficiency, nephrotic syndrome, etc.).

The product contains sucrose, therefore patients with rare hereditary problems of fructose intolerance, glucose-galactose malabsorption, or sucrase isomaltase insufficiency, should not take this medicine. The sucrose content is 2.95 g per sachet: this must be taken into account in case of diabetes or low-calorie diets.

Pregnancy and breastfeeding
The product should not be used during pregnancy and breastfeeding

Expiry and retention
Check the expiration date indicated on the package. The expiry date indicated on the package refers to the product in intact packaging, correctly stored.

Warning: do not use the medicine after the expiry date indicated on the package.

Composition
Geffer Granulate contains:
Active ingredient: metoclopramide hydrochloride 5 mg, dimethicone 50 mg, potassium citrate 94.45 mg, citric acid 670 mg, tartaric acid 152 mg, sodium bicarbonate 1050 mg
Excipients: Orange flavor, sucrose

This sheet has been prepared using information provided by the manufacturer. It should be noted that the packaging of the products is susceptible to periodic renewals by the pharmaceutical companies, therefore the photo of the product may not be updated; the only data to be trusted is the unique ministerial code (Minsan).