


Ask a doctor about a prescription for MOSEGOR 0.5 mg/10 ml ORAL SOLUTION
Package Leaflet: Information for the User
Mosegor0.5 mg/10 ml Oral Solution
Pizotifen
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the Package Leaflet
The active substance of Mosegor is pizotifen, which has an appetite-stimulating effect that promotes weight gain in patients with low body weight (whose appetite has been reduced or lost).
Mosegor is used for the treatment of loss of appetite in patients with low body weight as a complement to the treatment of the disease that causes weight loss.
Follow your doctor's instructions carefully. These may differ from the general information included in this leaflet.
Do not take Mosegor
Warnings and precautions
Tell your doctor if you have or have had any of these conditions:
If you experience the symptoms described above while taking Mosegor, tell your doctor immediately.
If you are in any of the situations described, tell your doctor before taking the medicine.
Children and adolescents
Mosegor should not be given to children under 2 years of age.
Interaction of Mosegor with other medicines
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines.
It is important that your doctor knows if you are taking:
Mosegor with food, drink, and alcohol
Consuming alcohol may increase the sedative effects of this medicine.
Pregnancy and breastfeeding
Pregnancy
Tell your doctor if you are or think you may be pregnant.
Experience with Mosegor in pregnancy is limited, so it should only be used in special circumstances, which your doctor will discuss with you.
Breastfeeding
Do not take the medicine while breastfeeding.
Driving and using machines
This medicine may cause drowsiness, dizziness, and other effects on the brain, so you should drive and use machines with caution. If you feel sleepy, do not drive or perform any activity that requires you to be alert (such as using tools or machines) until you feel well enough to avoid any risk to yourself and others.
Mosegor contains ethanol
Mosegor contains sucrose
Mosegor contains propyl parahydroxybenzoate and methyl parahydroxybenzoate
Mosegor contains sorbitol
This medicine contains 10 g of sorbitol per 20 ml dose. Sorbitol is a source of fructose. If your doctor has told you that you (or your child) have an intolerance to certain sugars, or have been diagnosed with hereditary fructose intolerance (HFI), a rare genetic disease in which the patient cannot break down fructose, consult with your doctor before taking this medicine. Sorbitol may cause gastrointestinal upset and a mild laxative effect.
Follow your doctor's instructions for taking Mosegor exactly. If you are unsure, consult your doctor or pharmacist again. Do not take a higher dose than your doctor has indicated.
The initial dose in adults is 0.5 mg (10 ml of the solution) per day, which may be gradually increased to 0.5 mg (10 ml of the solution) three times a day.
Use in children (from 2 to 12 years)
Low initial doses will be gradually increased to reach a maintenance dose of 0.025 mg/kg per day. The resulting total dose may be divided into 2 or 3 daily doses, as prescribed by your doctor.
These are the approximate daily doses:
In adolescents over 13 years old with a body weight over 40 kg, the same dose as for an adult can be administered, i.e., starting with 0.5 mg per day and gradually increasing the dose to 0.5 mg three times a day.
If you take more Mosegor than you should
If you have accidentally taken too much Mosegor solution, contact your doctor immediately as medical attention may be necessary. You can also call the Toxicology Information Service, phone number 91 562 04 20, indicating the medicine and the amount taken.
If you forget to take Mosegor
If you forget to take a dose of Mosegor, take it as soon as possible. If it is only 4 hours or less until the next dose, wait until the scheduled time and take the medicine according to the initial schedule. Do not take a double dose to make up for forgotten doses. If you are unsure, consult your doctor.
If you stop taking Mosegor
Do not change or stop your medication without asking your doctor. Your doctor may recommend gradually reducing the dose before stopping treatment. This is done to avoid worsening your health condition and reduce the risk of withdrawal symptoms such as depression, tremors, nausea, anxiety, feeling unwell, dizziness, sleep disorders, and weight loss.
If you have any doubts about the use of this medicine, ask your doctor or pharmacist.
Like all medicines, Mosegor can cause side effects, although not everybody gets them.
These side effects may occur with certain frequencies, which are described below:
Very common | Affect more than 1 in 10 patients |
Common | Affect between 1 and 10 in 100 patients |
Uncommon | Affect between 1 and 10 in 1,000 patients |
Rare | Affect between 1 and 10 in 10,000 patients |
Very rare | Affect less than 1 in 10,000 patients |
Frequency not known | Cannot be estimated from the available data |
Some side effects may be serious. If you notice any of them, tell your doctor immediately:
Rare:
Very rare:
Frequency not known:
Other side effects:
Very common:
Common:
Uncommon:
Rare:
Frequency not known:
If you experience side effects, talk to your doctor or pharmacist, even if it is a side effect not listed in this leaflet.
Composition of Mosegor
Appearance of the product and pack contents
Bottle with 200 ml and dosing cup.
Marketing authorization holder
ETHYX PHARMACEUTICALS
19 rue Duquesne
69006 Lyon
France
Manufacturer
DELPHARM ORLEANS
5 avenue de concyr
45071 Orleans
France
This leaflet was approved in
May 2022
Detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.es/
Discuss dosage, side effects, interactions, contraindications, and prescription renewal for MOSEGOR 0.5 mg/10 ml ORAL SOLUTION – subject to medical assessment and local rules.