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Tell your doctor right away if you have any serious side effects, including: signs of low potassium level in the blood such as muscle cramps, weakness, irregular heartbeat This medication can cause low blood sugar hypoglycemia This may occur if you do not consume enough calories from food or if you do unusually heavy exercise.it is essentially 'sodium-free'.
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Before using SoloStar, the instructions for use included in the package leaflet must be read carefully. SoloStar has to be used as recommended in these instructions for use see section 6.Do not use other GLP-1 RAs. Accidental mix-ups between insulin products have been reported. Instruct patients to always check the label before administration.
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Please note: the Federal Employees Health Benefits FEHB Program is not a federal or state government health care program for purposes of the savings program. Void where prohibited by law.Do NOT use a syringe to remove Toujeo from your pen.
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Any change of insulin should be made cautiously and only under medical supervision.But many who rely on insulin still struggle. Large numbers resort to rationing a dangerous and sometimes deadly practice.
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Lantus should be administered once a day at the same time every day. Limitations of Use: Lantus is not recommended for the treatment of diabetic ketoacidosis.Changes in insulin regimen may result in hyperglycemia or hypoglycemia. Repeated insulin injections into areas of lipodystrophy or localized cutaneous amyloidosis may result in hyperglycemia; sudden change in the injection site to unaffected lantus solostar 3 ml has been reported to result in hypoglycemia.
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During admission, the patient required significantly less insulin Lantus 15 units at bedtime and NovoLOG 4 to 6 units before each meal than he had been prescribed before his admission. Although it may seem improbable that this misadministration happened for more than a lantus solostar 3 ml, it did happen.Do not inject this medicine into skin that is damaged, tender, bruised, pitted, thickened, scaly, or has a lantus solostar 3 ml or hard lump.
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Macrovascular Outcomes: Clinical studies have not shown macrovascular risk reduction with SOLIQUA. he most common adverse reactions reported in 5% of patients treated with SOLIQUA 100/33 include hypoglycemia, nausea, nasopharyngitis, diarrhea, upper respiratory tract infection, and headache.ach vial contains 5 ml of solution for injection, equivalent to 500 units, or 10 ml of solution for injection, equivalent to 1000 units.
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378 mg insulin glargine. The 3 mL prefilled pen presentation contains the following inactive ingredients per mL: 30 mcg zinc, 2.Do not withdraw SOLIQUA 100/33 from the pen with a syringe.
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