Potenciator
POTENCIATOR® 5g Arginine aspartate
DOSAGE FORM: Oral solution in drinkable ampoules.
COMPOSITION: Each ampoule for drinking contains: Arginine aspartate 5 g.
Excipients: 70% sorbitol solution (2 g), saccharose (1.3 g), monohydrate citric acid, saccharin sodium (13 mg), caramel aroma, caramel colouring (E150), potassium sorbate (E202), deionized water, methylparaben (E218), propylparaben (E216), s.q.
PHARMACOLOGICAL ACTION: The components of POTENCIATOR are two amino acids which are involved in the replenishment of protein reserves. INDICATIONS: Prevention of deficiency states of amino acids caused by an insufficient protein intake due to vegetarian diets, lack of appetite, convalescence. INTERACTION WITH OTHER DRUGS AND FOODS: None reported.
CONTRAINDICATIONS: Hypersensitivity or allergy to any of the components of POTENCIATOR. Severe renal or liver failure.
PRECAUTIONS: Patients with urinary retention problems must only take POTENCIATOR under medical control. POTENCIATOR must not be taken continuously. If symptoms worsen or persist, consult with your doctor.
INCOMPATIBILITIES: None reported.
ADVERSE REACTIONS: In some cases, allergic reactions occur. If any other adverse reaction not previously described is seen, consult with your doctor or pharmacist.
WARNINGS: Use during pregnancy and nursing
If you are pregnant or you think you could be pregnant, consult your doctor before taking this drug. The use of drugs during pregnancy can be dangerous for the embryo or fetus and must be monitored by your doctor.
Nursing women must not use this drug without consulting their doctor.
Warning regarding excipients: This drug contains 1.3 g of saccharose per ampoule, which should be taken into account by diabetic patients.
This drug contains 1.4 g of sorbitol per drinkable ampoule. It may cause upset stomach and diarrhoea. It should not be used in patients with hereditary fructose intolerance. The drug contains potassium sorbate as an excipient, which is harmful to patients with low potassium diets. Excess potassium, following oral ingestion, may cause stomach upset and diarrhoea.
DOSE AND METHOD OF ADMINISTRATION: Oral way.
Children under 2 years: is not recommended the use of this drug. Children from 2 to 6 years: only if prescribed by your doctor. Children from 6 to 12 years: 1 ampoule or the dose recommended by your doctor. Above 12 years and Adults: 1 ampoule twice a day.
The contents of the ampoule can be taken diluted with some water or fruit juice at the end of the main meals.
INSTRUCTIONS FOR ADEQUATE ADMINISTRATION OF THE PREPARATION:
- Detach the ampoule.
- Tear the tab at the top of the ampoule with a twisting motion.
- After turning it upside down, press the ampoule and pour its contents in a glass.
TREATMENT IN CASE OF INTOXICATION OR OVERDOSE: Continued or accidental intake of large doses may cause gastrointestinal discomfort (diarrhea, nausea, vomiting). Consult your doctor.
In case of overdosage or accidental intake, consult the doctor.
PRESENTATION: Package containing 20 ampoules.
No medical prescription required. Do not store above 30°C. Keep drugs out of reach of children. Fabricante y titular / Fabricant et titulaire / Manufacturer and Product licence holder:
FAES FARMA, S.A.
Máximo Aguirre, 14 48940 - Leioa (Vizcaya)
ESPAÑA / ESPAGNE / SPAIN
