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Generic Name: fluconazole, note: This document contains side effect information about fluconazole. Some of diflucan for tinea pedis the dosage forms listed on this page may not apply to the brand name Diflucan. In Summary, more frequent side effects diflucan for tinea pedis include: vomiting. See below for a comprehensive list of adverse effects. For the Consumer, applies to fluconazole : oral capsule, oral powder for suspension, oral tablet. Other dosage forms: Along with its needed effects, fluconazole (the active ingredient contained. Diflucan ) may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention. Check with your doctor immediately if any of the following side effects occur while taking fluconazole: Rare, chills clay-colored stools cough dark urine diarrhea difficulty with swallowing dizziness fast heartbeat fever general feeling of tiredness or weakness headache hives, itching, or skin rash large, hive-like. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them: Less common Belching change diflucan for tinea pedis in taste or bad, unusual, or unpleasant (after) taste heartburn indigestion stomach discomfort or upset Incidence. Changes in renal and hematological function test results and hepatic abnormalities reported during therapy with this and comparative agents in some patients, primarily those with serious underlying diseases (e.g., aids, cancer clinical significance and relationship to therapy unclear. During clinical trials of single-dose therapy, side effects possibly related to therapy were reported in 26 of patients using this drug and 16 of patients using active comparative agents. The most common side effects reported in patients receiving a single 150 mg dose of this drug for vaginitis were headache, nausea, and abdominal pain. Most side effects were of mild to moderate severity. During clinical trials of multiple-dose therapy, side effects were reported in 16 of patients. Therapy discontinuation occurred.5 and.3 of patients due to adverse clinical events and laboratory test abnormalities, respectively. Clinical side effects were reported more often in HIV -infected patients than in non-HIV-infected patients (21 versus 13 but the patterns in both groups were similar. Ref Nervous system Rare cases of seizures have been reported, but a causal relationship was difficult to establish, since some of these patients had cryptococcal meningitis or severe underlying disease. Nonetheless, at least 1 case of seizure following a 100 mg oral dose has been reported. Seizures, dizziness, paresthesia, somnolence, tremor, and vertigo have also been reported during postmarketing experience. Ref Very common (10 or more Headache (up to 13) Uncommon (0.1 to 1 Seizures, dizziness, paresthesia, somnolence, vertigo, visual field defect, taste perversion, hyperkinesia, hypertonia Rare (less than.1 Tremor Frequency not reported: Dysesthesias Ref Gastrointestinal Very common (10 or more Nausea, abdominal pain. Ref Hepatic Fatal hepatic reactions have occurred primarily in patients with serious underlying medical conditions (primarily aids or malignancy) and often taking multiple concomitant medications. One reported patient with aids experienced acute hepatic necrosis and hepatic failure about 3 weeks after starting this drug. Transient hepatic reactions have been reported in patients with no other identifiable risk factors. Liver function returned to baseline after stopping this drug. Serum transaminase elevations (greater than 8 times the upper limit of normal 8 x ULN; about 1) and statistically significant increases in AST have been reported.
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