NA | Cystadane [Orphan Europe SARL] | BioPortfolio

13:15 EST 27th January 2019 | BioPortfolio

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Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.

What is in this leaflet

1. What Cystadane is and what it is used for

Cystadane contains betaine anhydrous which is intended to be an adjunctive treatment of homocystinuria, an inherited (genetic) disease where the amino acid methionine cannot be broken down completely by the body. Methionine is present in regular food protein (e.g. meat, fish, milk, cheese, eggs). It is converted into homocysteine which is then normally converted into cysteine during digestion. Homocystinuria is a disease caused by the accumulation of homocysteine which is not converted to cysteine and is characterised by formation of clots in the veins, bone weakness, and skeletal and crystalline lens abnormalities. The use of Cystadane together with other treatments such as vitamin B6, vitamin B12, folate and a specific diet aims to reduce the elevated homocysteine levels in your body. 2. What you need to know before you take Cystadane Do not take Cystadane If you are allergic to betaine anhydrous. Warnings and precautions Talk to your doctor or pharmacist before taking Cystadane. If you notice side effects like headaches, vomiting or a change in your vision and you are of the homocystinuria subtype called CBS (cystathionine beta-synthase deficiency), please contact your doctor immediately, they could be signs of a swelling in the brain (cerebral oedema). In that case your doctor will monitor your methionine level in your body and may review your diet. Your treatment with Cystadane may need to be interrupted. If you are treated with Cystadane and with an amino-acid mixture and if you need to take other medicines at the same time, leave 30 minutes between the intake (see “section “Other medicines and Cystadane”). Other medicines and Cystadane Tell your doctor if you are taking, have recently taken or might take any other medicines. If you are taking amino-acid mixture or medicines such as vigabatrin or Gaba analogues (medicine used to treat epilepsy), please tell your doctor as they might interact with your treatment with Cystadane. Pregnancy and breast-feeding If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor for advice before taking this medicine. Your doctor will decide if you can use this medicine during pregnancy and breast-feeding. Driving and using machines Cystadane has no or negligible influence on the ability to drive and use machines.

3. How to take Cystadane The use of this medicine will be supervised by a doctor experienced in the treatment of patients with homocystinuria. Always take this medicine exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure. The recommended dose in children and adults is 100mg/kg/day divided in 2 dosesper day. In some patients doses above 200 mg/kg/day were needed to reach therapeutic goals. Your doctor may adapt the dose depending on your laboratory values. You will therefore need regular blood tests to determine the correct daily dose. You should take Cystadane orally (by mouth). To measure the dose:

Mix the measured dose of powder with water, juice, milk, formula or food until completely dissolved and ingest immediately after mixing. If you take more Cystadane than you should If you accidentally take too much Cystadane, talk to a doctor or pharmacist immediately. If you forget to take Cystadane Do not take a double dose to make up for forgotten doses. If you forget to take a dose take it as soon as you remember it and continue the next dose as planned.

If you stop taking Cystadane Do not stop the treatment without consulting your doctor. Contact your doctor or pharmacist before stopping. If you have any further questions on the use of this medicine, ask your doctor or pharmacist. 4. Possible side effects Like all medicines, this medicine can cause side effects, although not everybody gets them. The most commonly side effect when taking Cystadane which may affect more than 1 in 10 people (frequency very common) is elevated levels of methionine in the blood. Methionine level can be related to swelling in the brain (cerebral swelling), which may affect up to 1 in 100 people (frequency uncommon). If you experience morning headaches with vomiting and/or visual changes, contact immediately your doctor (they could be signs of a swelling in the brain).

Gastrointestinal disorders like diarrhoea, nausea, vomiting, stomach discomfort and inflammation of the tongue may occur uncommonly (may affect up to 1 in 100 people). Other uncommon side effects (may affect up to 1 in 100 people) may include decreased appetite (anorexia), agitation, irritability, hair loss, hives, skin odour abnormal, lack of control over passing urine (urinary incontinence). Reporting of side effects If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system listed in Appendix. By reporting side effects you can help provide more information on the safety of this medicine. 5. How to store Cystadane 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 bottle label and the carton after EXP. The expiry date refers to the last day of that month.

Do not store above 25°C. Keep the bottle tightly closed in order to protect from moisture. After the first opening of the bottle, the medicine should be used within 3 months. Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment. 6. Contents of the pack and other information What Cystadane contains

What Cystadane looks like and contents of the pack Cystadane is a white crystalline free flowing powder. It is presented in bottles with child resistant closures. Each bottle contains 180 g of powder. Each carton contains one bottle and three measuring spoons.

Marketing Authorisation Holder Orphan Europe SARL Immeuble “Le Wilson” 70, avenue du General de Gaulle F-92 800 Puteaux France Manufacturer Orphan Europe SARL Immeuble “Le Wilson” 70, avenue du Général de Gaulle F-92800 Puteaux France For any information about this medicine, please contact the local representative of the Marketing Authorisation Holder. This leaflet was last revised in 8/12/2016 Detailed information on this medicine is available on the European Medicines Agency web site: There are also links to other websites about rare diseases and treatments.

Orphan Europe Ltd. Tel : + 44 (0)14 9141 4333 United Kingdom - Ireland



Reporting of side effects Yellow Card Scheme Website: or search for MHRA Yellow Card in the Google Play or Apple App Store


22 December 2017

Subject: Temporary importation of CYSTADANE® (betaine anhydrous for oral solution) to address impending shortage

Dear Health Care Provider,

There has been a manufacturing issue with the CYSTADANE® (betaine anhydrous for oral solution) approved for use and distribution in the United States (“U.S.-labeled CYSTADANE”), which has resulted in an interim shortage of this product in the U.S. market.

In order to alleviate the shortage of CYSTADANE in the U.S., Recordati Rare Diseases Inc. (Recordati) is coordinating with the U.S. Food and Drug Administration (FDA) to increase the availability of CYSTADANE. Recordati has initiated temporary importation of its CYSTADANE product approved for use in the United Kingdom into the U.S. market. This product is manufactured by Orphan Europe SARL in France. At this time, no other entity except Recordati, as the U.S. agent of Orphan Europe SARL, is authorized to import or distribute these products in the United States. FDA has not approved the product manufactured by Orphan Europe SARL’s manufacturing facility in France. The imported CYSTADANE is lot CYP1705. It will be dispensed by the U.S. specialty pharmacy, AnovoRx Group LLC.

There are some key differences between the FDA-approved CYSTADANE and the imported CYSTADANE.

A copy of the FDA-approved full prescribing information is being distributed with the imported CYSTADANE. Please refer to the FDA-approved package insert for full prescribing information. Storage conditions are the same as that of the FDA-approved product. Store at room temperature, 15º – 30ºC (59º – 86ºF). CYSTADANE is for oral use only. Protect from moisture. Keep this and all medications out of the reach of children.

U.S. FDA-approved Indication

CYSTADANE (betaine anhydrous for oral solution) is a methylating agent indicated for the treatment of homocystinuria to decrease elevated homocysteine blood levels. Included within the category of homocystinuria are:

For reporting of adverse events and more information

Any adverse effects or medication issues resulting from the use of this drug or quality issues should be reported to Recordati Rare Diseases Inc. at 1-888-575-8344.

Adverse events or quality problems experienced with the use of this product may also be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax:

Important Safety Information

We are committed to helping address patients’ unmet needs through our corporate mission. If you have questions or concerns regarding this product, please call AnovoRx Group, the specialty pharmacy that dispenses CYSTADANE, at 1‑888-487-4703 or Recordati Rare Diseases Medical Information at 1‑888-575-8344.

Steven R. Peltier

Vice President, Regulatory & Quality Compliance

Chief Compliance Officer

Recordati Rare Diseases Inc.

FDA-approved (U.S.) Bottle Label:

Imported (U.K.) Bottle Label:

Imported (U.K.) Carton:


1 g

Orphan Europe SARL

Immeuble “Le Wilson”

70 avenue du Général de Gaulle

F-92800 Puteaux

Cystadane 1 g oral powder.

Betaine anhydrous

1 g of powder contains 1 g of betaine anhydrous. 180 g of oral powder and three measuring spoons. Three measuring spoons (green, blue, pink) dispense 100mg, 150mg or 1g of betaine anhydrous. Lightly shake the bottle before opening. Read the package leaflet before use. ORAL USE. Keep out of the sight and reach of children. Do not store above 25°C. Keep the bottle tightly closed in order to protect from moisture. Medicinal product subject to medical prescription.

Shelf life after the first opening: 3 months




Orphan Europe SARL

Active Ingredients


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To assess the safety and efficacy of betaine in patients with NASH on markers of disease severity such as liver histology, liver biochemistries, and health related quality of life.

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