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Levitra dosage. In dose to 20 mg based on side effects and efficacy. Back pain was reported in 2.0% of patients treated with LEVITRA and 1.7% of patients on placebo. Placebo-controlled trials suggested a dose effect in the incidence of some adverse events (headache, flushing, dyspepsia, nausea, rhinitis) over the 5 mg, 10 mg, and 20 mg doses of LEVITRA. The following section identifies additional, less frequent events (<2%) reported during the clinical development of LEVITRA. Excluded from this list are those events that are infrequent and minor, those events that may be commonly observed in the absence of drug therapy, and those events that are not reasonably associated with the drug. BODY AS A WHOLE: anaphylactic reaction (including laryngeal edema), asthenia, face edema, pain AUDITORY: tinnitus CARDIOVASCULAR: angina pectoris, chest pain, hypertension, hypotension, myocardial ischemia, myocardial infarction, palpitation, postural hypotension, syncope, tachycardia DIGESTIVE: abdominal pain, abnor
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Mal liver function tests, diarrhea, dry mouth, dysphagia, esophagitis, gastritis, gastroesophageal reflux, GGTP increased, vomiting MUSCULOSKELETAL: arthralgia, back pain, myalgia, neck pain NERVOUS: hypertonia, hypesthesia, insomnia, paresthesia, somnolence, vertigo RESPIRATORY: dyspnea, epistaxis, pharyngitis SKIN AND APPENDAGES: photosensitivity reaction, pruritus, rash, sweating OPHTHALMOLOGIC: abnormal vision, blurred vision, chromatopsia, changes in color vision, conjunctivitis (increased redness of the eye), dim vision, eye pain, glaucoma, photophobia, watery eyes UROGENITAL: abnormal ejaculation, priapism (including prolonged or painful erections) POST-MARKETING EXPERIENCE Ophthalmologic Non-arteritic anterior ischemic optic neuropathy (NAION), a cause of decreased vision including permanent loss of vision, has been reported rarely post-marketing in temporal association with the use of phosphodiesterase type 5 (PDE5) inhibitors, including LEVITRA. Most, but not all, of these pa
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