Ülke: Birleşik Krallık
Dil: İngilizce
Kaynak: MHRA (Medicines & Healthcare Products Regulatory Agency)
Ferrous sulfate
Wallace Manufacturing Chemists Ltd
B03AA07
Ferrous sulfate
125mg/1ml
Oral drops
Oral
No Controlled Drug Status
Valid as a prescribable product
BNF: 09010101; GTIN: 05034593020409
# wallace In this leaflet 1. What Ironorm Drops are and what do they do? 2. What should I know before using Ironorm Drops? 3. How do I use Ironorm Drops? 4. Do Ironorm Drops have any side effects? 5. How do I store Ironorm Drops? 6. Further Information. 1. What Ironorm Drops are and what do they do? The name of your medicine is Ironorm Drops. Ironorm Drops contain Ferrous Sulfate. It is used to prevent or treat iron deficiency anaemia. 2. What should I know before using Ironorm Drops? YOU SHOULD NOT USE THIS MEDICINE IF YOU: # Are sensitive to any of the ingredients (full list provided in Section 6). # You suffer from an inherited condition of abnormal iron metabolism. # You have an active peptic ulcer. # You are undergoing repeated blood transfusions. # You suffer from a severe stomach upset or ulcerative colitis. # You have been diagnosed with a haemolytic anaemia which are anaemias that cause break down of the red blood cells. TALK TO YOUR DOCTOR OR PHARMACIST BEFORE TAKING THIS MEDICINE IF YOU: # Have had a recent operation on your stomach. # Have previously suffered from a peptic ulcer. # You are already receiving treatment for other forms of anaemia. # You suffer from intestinal blockages. # You are elderly (there is an increased risk of intestinal blockage). IF YOU HAVE RECENTLY GIVEN BIRTH: # Treatment is not normally required more than 1 or 2 months after childbirth. IS IT SAFE TO DRIVE OR OPERATE MACHINERY AFTER TAKING IRONORM DROPS? Ironorm Drops do not affect your ability to drive or operate machinery. ARE THERE ANY MEDICINES OR FOODS THAT INTERACT WITH IRONORM DROPS? Ironorm Drops may react with other medicines you are taking. TALK TO A PHARMACIST OR DOCTOR IF YOU ARE TAKING THE FOLLOWING SINCE THEY WILL REDUCE EACH OTHER’S POTENCY: # Tetracyclines, a type of antibiotic. # Antacids. # Cholestyramine, used to remove bile from the gut. It is sometimes used to reduce blood cholesterol levels. # Penicillamine, a treatment for rheumatoid arthritis and a few other rare inherited conditions. TALK TO A PHA Belgenin tamamını okuyun
OBJECT 1 IRONORM DROPS Summary of Product Characteristics Updated 06-Jan-2017 | Wallace Manufacturing Chemists Ltd 1. Name of the medicinal product IRONORM DROPS 2. Qualitative and quantitative composition Each ml contains:- Ferrous Sulfate BP 125mg (equivalent to 25mg Iron per ml). 3. Pharmaceutical form Solution (Oral Drops). 4. Clinical particulars 4.1 Therapeutic indications For prevention and treatment of iron deficiency anaemias. 4.2 Posology and method of administration Oral administration. Prophylactic: A daily dose of 5 mg of elemental iron as prophylactic iron supplementation for babies of low birth weight who are solely breast-fed is recommended. Higher doses up to 2mg/kg of elemental iron per day might be needed to cover the needs of growing exclusively breastfed infants. Supplementation is started 4-6 weeks after birth and continued until mixed feeding is established. Older infants and children to 6 years: 0.5 – 1.2 ml per day (12.5 – 30 mg elemental iron). Older children: 2.4 ml per day (60 mg elemental iron). Adults and Elderly: 2.4 – 4.8 ml per day (60 – 120 mg of elemental iron) Therapeutic: Paediatric: 0.12ml to 0.24ml (3mg – 6mg elemental iron) per kg body weight, up to a maximum of 8ml (200mg elemental iron) given daily in two or three divided doses. Adults: 4.0 ml once or twice per day (100 – 200 mg elemental iron) 4.3 Contraindications • Hypersensitivity to the product or ingredients • Haemosiderosis and haemocromatosis • Active peptic ulcer • Repeated blood transfusion • Regional enteritis and ulcerative colitis • Haemolytic anaemias 4.4 Special warnings and precautions for use • Patients post-gastrectomy have poor absorption of iron. • Caution is advised when prescribing iron preparations to individuals with history of peptic ulcer. • Duration of treatment should generally not exceed 1-2 months after end of pregnancy. • Coexisting deficiency of dietary vitamin B12 should be ruled out since combined deficiency produces microcytic blood film. • Care should b Belgenin tamamını okuyun