Cyanocobalamin(Vitamin B12)
Ankermann contains cyanocobalamin, also known as Vitamin B12.
Most people get enough Vitamin B12 through their diet, but if you have had stomach surgery, have certain stomach or intestinal disorders, follow a strict diet, or take certain medications, your body may not get enough Vitamin B12.
This medicine is used to treat Vitamin B12 deficiency and to maintain treatment in adult patients:
This medicine is also used to treat Vitamin B12 deficiency caused by reduced intake (e.g., in a vegetarian diet) in adults.
Before starting to take Ankermann, discuss it with your doctor or pharmacist.
Before starting treatment, your doctor should diagnose your condition to determine the cause of the deficiency. This includes checking the function of the digestive tract. The doctor will decide whether Vitamin B12 absorption from food is insufficient and whether oral supplementation with this medicine is necessary.
Due to the serious nature of the disease, your doctor will likely want to monitor your response to this medicine during the first 3 months of treatment. This will likely include blood tests. If you follow the treatment plan, treatment may last a lifetime, depending on the underlying disease.
If you need regular dialysis, your doctor should regularly perform blood tests and may need to reduce the dose of this medicine.
If you have a folic acid deficiency, it may weaken your response to treatment.
In this case, you should take folic acid supplements in parallel with this medicine.
Ankermann contains 1000 micrograms of cyanocobalamin per tablet. If you are going to have laboratory tests, tell your doctor or laboratory staff that you are taking this medicine, as cyanocobalamin may affect the results of such tests (including blood, urine, skin tests with allergens, etc.) due to its red color. This medicine may affect the determination of intrinsic factor antibodies.
Do not give this medicine to children and adolescents under 18 years of age, as the safety and efficacy of this medicine in children and adolescents have not yet been established.
Tell your doctor or pharmacist about all medicines you are taking, have recently taken, or plan to take, including those available without a prescription.
The effect of Ankermann may be altered by:
Alcohol may affect the absorption of this medicine into the body.
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine. As a precautionary measure, it is recommended to avoid taking this medicine during pregnancy, unless the woman's condition requires treatment with cyanocobalamin.
This medicine can be used during breastfeeding.
Ankermann should not affect your ability to drive or use machines.
Lactose monohydrate and sucrose
If you have been diagnosed with intolerance to some sugars, consult your doctor before taking this medicine.
Macrogolglycerol hydroxystearate
May cause stomach upset and diarrhea.
Sodium
This medicine contains less than 1 mmol of sodium (23 mg) per tablet, which means it is essentially "sodium-free".
Always take this medicine exactly as your doctor or pharmacist has told you. If you are not sure, ask your doctor or pharmacist.
The recommended daily dose is 1 tablet of Ankermann. This corresponds to 1000 micrograms of cyanocobalamin in the following indications:
Patient with severe hematological or neurological symptoms of Vitamin B12 deficiency must initially be treated with parenteral Vitamin B12 until the Vitamin B12 level in the blood is normalized.
If oral Vitamin B12 is well tolerated, there are no restrictions on the duration of treatment in the case of megaloblastic anemia or malabsorption disorder.
Regular monitoring of the response to treatment is necessary (see also section 2 Warnings and precautions).
In patients with moderate renal impairment, Ankermann can be taken using the usual recommended dose for adults. In the case of severe renal impairment, a dose reduction is recommended. Additionally, regular monitoring of Vitamin B12 levels in the blood is necessary.
There are no data on the use of Ankermann in patients with hepatic impairment. If you have liver disease, inform your doctor.
Method of administration
Ankermann tablets should be swallowed whole, with a sufficient amount of water, preferably in the morning, on an empty stomach. The duration of treatment depends on the response to treatment. Your doctor will determine the appropriate dose for you based on regular check-ups.
In the event of an overdose of Ankermann, consult your doctor, who will decide on the appropriate course of action. No cases of overdose have been reported.
There is no known antidote. In the event of an overdose, symptomatic treatment should be used.
If you miss a dose of Ankermann, take it as soon as possible, unless it is almost time for the next dose. In this case, take the next dose at the scheduled time. Do not take a double dose to make up for a missed dose.
Always consult your doctor before stopping treatment with Ankermann.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Like all medicines, Ankermann can cause side effects, although not everybody gets them.
If you experience any side effects, including those not listed in this leaflet, tell your doctor or pharmacist. Side effects can be reported directly to the Department of Drug Safety Monitoring, Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products, Al. Jerozolimskie 181 C, 02-222 Warsaw, Tel.: +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.
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the carton after EXP. The expiry date refers to the last day of that month.
Do not store above 25°C.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help protect the environment.
The active substance is:
1000 micrograms of cyanocobalamin (synthetic form of Vitamin B12).
The other ingredients are:
lactose monohydrate, povidone K30, croscarmellose sodium, stearic acid 50 (stearic acid and palmitic acid), AquaPolish P white*, sucrose, talc, kaolin, calcium carbonate, titanium dioxide (E 171), arabic gum dispersion dried, macrogol 6000, macrogolglycerol hydroxystearate 40, sodium lauryl sulfate (E487), montan glycol wax.
(*The composition of the "AquaPolish P white" coating is: hypromellose, hydroxypropylcellulose, stearic acid 50 (stearic acid and palmitic acid), talc, medium-chain triglycerides, titanium dioxide (E 171)).
Round, biconvex, white chewable tablets with a diameter of approximately 9.8 mm.
The carton contains 10, 25, 30, 50, 60, 90, or 100 chewable tablets in PVC/PVDC/Aluminum blisters.
Not all pack sizes may be marketed.
Wörwag Pharma GmbH & Co. KG
Flugfeld-Allee 24
71034 Böblingen
Germany
Artesan Pharma GmbH & Co. KG
Wendlandstraße 1
29439 Lüchow
Germany
To obtain more detailed information on this medicine, contact the local representative of the marketing authorization holder:
Woerwag Pharma Polska Sp. z o.o.
ul. Józefa Piusa Dziekońskiego 1
00-728 Warsaw
tel. (+48) 22 863 72 81
fax (+48) 22 877 13 70
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