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Manufactured by Merck and generically referred to as sitagliptin, Januvia® is an oral diabetes medication that, when taken in conjunction with a healthy diet and regular exercise, can be effective at helping type-2 diabetes patients control their blood glucose (sugar) levels. Patients with type-1 diabetes and/or those who have diabetic ketoacidosis (a potentially fatal diabetes complication) should not take Januvia®.
Januvia® was approved by the Food and Drug Administration (FDA) in 2006 and, despite its effectiveness, has been reported to cause a range of mild to potentially fatal side effects.
To minimize the risk of developing any of these side effects, it's crucial that Januvia® patients:
In most cases, Januvia® side effects are treatable, fleeting and minor and may include any combination of:
As with other type-2 diabetes medications, Januvia® can cause some patients to experience abnormally and dangerously low blood sugar levels (clinically known as hypoglycemia), the symptoms of which may include (but are not limited to) heart palpitations, dizziness, disorientation, fatigue, double vision and irritability.
Severe allergic reaction to Januvia® is among the serious side effects of this diabetes medication, and it requires immediate medical care to prevent fatality. Breathing difficulties, facial or tongue inflammation, and/or skin rash or hives are symptoms of severe Januvia® allergic reaction.
A recent study conducted at the University of California, Los Angeles (UCLA) has also found a potential link between taking Januvia® and having an increased risk of developing:
Those who have suffered as a result of taking Januvia® will likely be entitled to compensation for their pain, losses, medical bills, lost wages, etc. To find out if you have a defective drug case against Merck, meet with a skilled Januvia® attorney for a complimentary initial consult.
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