It’s manufactured and marketed by Janssen Pharmaceuticals, Inc., and was Initially hailed as a “miracle drug” for the treatment of Type 2 diabetes.. In males, discontinuations due to genital mycotic infections occurred in 0% and 0.5% of patients treated with placebo and INVOKANA, respectively.In the pooled analysis of 8 randomized trials evaluating glycemic control, phimosis was reported in 0.3% of uncircumcised male patients treated with INVOKANA and 0.2% required circumcision to treat the phimosis [seeIn all glycemic control trials, hypoglycemia was defined as any event regardless of symptoms, where biochemical hypoglycemia was documented (any glucose value below or equal to 70 mg/dL). Call your doctor for medical advice about side effects.
FDA. Our kidneys work hard to do some FDA "FDA warns about rare occurrences of a serious infection of the genital Call your doctor for medical advice about side effects. Vaginal itching. Male genital mycotic infections occurred more commonly in uncircumcised males and in males with a prior history of balanitis or balanoposthitis. In females, discontinuation due to genital mycotic infections occurred in 0% and 0.7% of patients treated with placebo and INVOKANA, respectively [seeIn the pool of four placebo-controlled clinical trials, male genital mycotic infections (e.g., candidal balanitis, balanoposthitis) occurred in 0.7%, 4.2%, and 3.8% of males treated with placebo, INVOKANA 100 mg, and INVOKANA 300 mg, respectively.
O 02. Trademarks are those of their respective owners. You may report side effects to FDA at 1-800-FDA-1088.The following important adverse reactions are described below and elsewhere in the labeling:Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to the rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice.The data in Table 2 is derived from four 26-week placebo-controlled trials where INVOKANA was used as monotherapy in one trial and as add-on therapy in three trials. Baseline renal function was normal or mildly impaired (mean eGFR 88 mL/min/1.73 m²).Table 2 shows common adverse reactions associated with the use of INVOKANA. See below for a comprehensive list of adverse effects. The total number of amputations among canagliflozin-treated patients (n=5790) was 221 compared with 69 in the placebo group (n=4344). You may have low blood sugar (hypoglycemia) and feel very hungry, dizzy, irritable, confused, anxious, or shaky. Mean changes (percent changes) from baseline in LDL-C relative to placebo were 4.4 mg/dL (4.5%) and 8.2 mg/dL (8.0%) with INVOKANA 100 mg and INVOKANA 300 mg, respectively. Invokana (canagliflozin)." "Product Information. Tell your doctor if you have any side effect that bothers you or that does not go away. This link is provided for your convenience.
Janssen Pharmaceuticals, Titusville, NJ. US Food and Drug Administration "Invokana and Invokamet (canagliflozin): Drug Safety Communication - New Information on Bone Fracture Risk and Decreased Bone Mineral Density. This copyrighted material has been downloaded from a licensed data provider and is not for distribution, except as may be authorized by the applicable terms of use.Things to remember when you fill your prescription.WebMD does not provide medical advice, diagnosis or treatment. Patients in CANVAS and CANVAS-R were followed for an average of 5.7 and 2.1 years, respectively [see In the CANVAS trial (mean duration of follow-up of 5.7 years) [see INVOKANA results in an osmotic diuresis, which may lead to reductions in intravascular volume. Thank you for visiting our site. US Food and Drug Administration "FDA Drug Safety Communication: FDA confirms increased risk of leg and foot amputations with the diabetes medicine canagliflozin (Invokana, Invokamet, Invokamet XR) Available from: URL: https://www.fda.gov/Drugs/DrugSafety/ucm557507.htm?source=govdelivery&" ([2017, May 16]):9.
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