Nicotinamide
it is used for
Vitamin PP belongs to the group of vitamin B. It participates in the transfer of hydrogen and electrons in cellular respiration, glycolysis, and lipid biosynthesis processes.
Vitamin PP plays an important role in carbohydrate, fat, protein, purine, and pyrimidine metabolism, as well as in the synthesis of high-energy compounds. Together with vitamin C and methionine, it accelerates the regeneration of visual purple. It stimulates liver and pancreas function, increases gastric juice secretion, enhances intestinal peristalsis, and plays an important role in skin, muscle, peripheral, and central nervous system metabolism. After oral administration, vitamin PP is well absorbed from the gastrointestinal tract.
Vitamin PP is excreted in the urine, mainly in the form of N-methyl derivatives; only a small amount is excreted unchanged.
Vitaminum PP 50 Polfarmex/Vitaminum PP 200 Polfarmex is indicated for use:
Due to the frequent co-occurrence of deficiencies of many vitamins from group B and proteins, it is also recommended to administer other vitamins from group B in therapeutic doses and to use a high-protein diet.
Before starting to use Vitaminum PP 50 Polfarmex/Vitaminum PP 200 Polfarmex, you should consult a doctor or pharmacist.
You should be particularly cautious when using Vitaminum PP 50 Polfarmex/Vitaminum PP 200 Polfarmex in patients:
You should tell your doctor or pharmacist about all medicines you are currently taking or have recently taken, as well as any medicines you plan to take.
Vitamin PP increases the risk of myopathy (muscle damage) when used concomitantly with cholesterol-lowering medicines from the statin group (simvastatin, pravastatin, and others).
If you are pregnant or breastfeeding, think you may be pregnant, or plan to have a child, you should consult your doctor or pharmacist before using this medicine.
The medicine does not affect the ability to drive and use machines.
If you have been diagnosed with an intolerance to some sugars, you should consult your doctor before taking the medicine.
This medicine should always be used according to the doctor's recommendations. If you have any doubts, you should consult a doctor or pharmacist.
If the symptoms indicate a slight deficiency of vitamin PP, or if the patient's diet is poor in vitamin for various reasons, a preventive dose of usually 1 to 2 tablets per day is administered.
Therapeutically, depending on the degree of deficiency, 2 to 3 tablets per day, exceptionally up to 5 tablets per day in divided doses.
The tablet should be swallowed, washed down with water. To avoid or reduce irritation of the gastrointestinal tract mucosa, the medicine should be taken after a meal.
The doctor may establish an individual dose depending on the patient's condition and the expected treatment time.
Symptoms of vitamin PP overdose may include headaches, tingling, itching of the head, tinnitus, nausea, occasionally jaundice, heart rhythm disturbances. Vitamin PP overdose is associated with a risk of liver damage.
You should contact your doctor immediately.
You should not take a double dose to make up for a missed dose.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The medicine is usually well tolerated.
Very rarely (in less than 1 in 10,000 people) skin redness, facial flushing, urticaria, and rash have been observed.
When using high doses of the medicine (3 to 6 g per day), the following may occur: headaches, dizziness, vision disturbances, nausea, vomiting, diarrhea, increased uric acid or glucose levels in the blood.
Cases of liver damage have been reported during long-term use or use of doses above 3 g/day.
If you experience any side effects, including any side effects not listed in this leaflet, you should tell your doctor or pharmacist. Side effects can be reported directly to the Department of Monitoring of Adverse Reactions to Medicinal Products of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products
Al. Jerozolimskie 181C
02-222 Warsaw
Phone: (22) 49 21 301
Fax: (22) 49 21 309
Website: https://smz.ezdrowie.gov.pl
Side effects can also be reported to the marketing authorization holder.
Reporting side effects will help gather more information on the safety of the medicine.
The medicine should be stored out of sight and reach of children.
Do not use this medicine after the expiry date stated on the carton and blister after: "EXP". The expiry date refers to the last day of the month.
There are no special precautions for storing the medicine.
Medicines should not be disposed of via wastewater or household waste containers. You should ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
The packaging contains 20 tablets in blisters.
Polfarmex S.A.
ul. Józefów 9
99-300 Kutno
Phone: 24 357 44 44
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