Země: Spojené státy
Jazyk: angličtina
Zdroj: NLM (National Library of Medicine)
Iron (UNII: E1UOL152H7) (Iron - UNII:E1UOL152H7), Folic Acid (UNII: 935E97BOY8) (FOLIC ACID - UNII:935E97BOY8), ascorbic acid (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R), pyridoxine Hydrochloride (UNII: 68Y4CF58BV) (PYRIDOXINE - UNII:KV2JZ1BI6Z), Cyanocobalamin (UNII: P6YC3EG204) (CYANOCOBALAMIN - UNII:P6YC3EG204), ZINC (UNII: J41CSQ7QDS) (ZINC - UNII:J41CSQ7QDS)
Trigen Laboratories, LLC
Iron
Iron 150 mg
ORAL
CORVITA™ 150 should not be used by patients with a known hypersensitivity to any of the listed ingredients. All iron compounds are contraindicated in patients with hemochromatosis, hemosiderosis, or hemolytic anemias.
CORVITA™ 150 tablets are supplied in unit dose packs of 100 (10 blister cards of 10 tablets each). PRODUCT CODE 13811-066-10
Dietary Supplement
CORVITA 150- IRON, FOLIC ACID, ASCORBIC ACID, PYRIDOXINE HYDROCHLORIDE, CYANOCOBALAMIN AND CITRATE TABLET TRIGEN LABORATORIES, LLC ---------- CORVITA 150 TABLETS SUPPLEMENT FACTS OTHER INGREDIENTS: Microcrystalline Cellulose, Pregelatinized Starch, Red Color Coating (Polyvinyl Alcohol, Polyethylene Glycol, FD&C Red #40 Lake, Talc, Titanium Dioxide), Croscarmellose Sodium, Magnesium Stearate, Stearic Acid GLUTEN-, LACTOSE- AND SUGAR-FREE CORVITA™ 150 is a prescription multivitamin/multimineral supplement used to improve the nutritional status of patients with iron deficiency CONTRAINDICATIONS TM CORVITA™ 150 should not be used by patients with a known hypersensitivity to any of the listed ingredients. All iron compounds are contraindicated in patients with hemochromatosis, hemosiderosis, or hemolytic anemias. WARNING: ACCIDENTAL OVERDOSE OF IRON-CONTAINING PRODUCTS IS A LEADING CAUSE OF FATAL POISONING IN CHILDREN UNDER 6. KEEP THIS PRODUCT OUT OF REACH OF CHILDREN. IN CASE OF ACCIDENTAL OVERDOSE, CALL A DOCTOR OR POISON CONTROL CENTER IMMEDIATELY. PRECAUTIONS GENERAL: Do not exceed recommended dose. The type of anemia and the underlying cause or causes should be determined before starting therapy with CORVITA™150. Since the anemia may be a result of a systemic disturbance, such as recurrent blood loss, the underlying cause or causes should be corrected, if possible. FOLIC ACID: Folic acid alone is an improper therapy in the treatment of pernicious anemia and other megaloblastic anemias where vitamin B12 is deficient. Folic acid in doses above 0.1 mg daily may obscure pernicious anemia in that hematologic remission can occur while neurologic manifestations remain progressive. Allergic sensitization has been reported following both oral and parenteral administration of folic acid. The patient’s medical conditions and consumption of other drugs, herbs, and/or supplements should be considered. PEDIATRIC USE: Safety and effectiveness in pediatric populations have not been established. GERIATRIC USE: Safety and Přečtěte si celý dokument