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Tamsulosin flomax 0.4 mg capsule 0.4 mg capsule emtamivir sulfate 50 mg/0.0175 mL twice daily 50 mg/0.0175 mL twice daily lamivudine (Depakote) 300 mg/day once daily 300 mg/day once daily zelivavir (2 doses) 30 mg a day as monotherapy or 4 doses add-on with at least 4 weeks between treatments Table 3. Common adverse reactions in randomized double-blind controlled studies. Adverse reactions that occurred by more than 10% of generic drug prices canada vs us patients and that might contribute to drug treatment discontinuation are listed. Also included the percentages of patients that responded to an antiviral agent within a 6-week treatment interval by at least 50%. (Adverse reactions are reported as absolute (±SE) numbers and percentages compared with published frequencies from the manufacturer's product labeling—both on basis of published data and on the basis of our individual experience with the drug.) Table 4. Antiviral drugs associated with serious adverse events. All event reports on clinicaltrials.gov are classified according to the International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM) (see definitions in "Additional Information" section at bottom of this page). Adverse Reactions that occurred in the studies conducted U.S. and Canada are listed first, followed by reports in which are from other countries. No serious adverse drug reactions occurred in any study (see "Study Design" and "Reporting of Clinical Trials" sections in "Additional Information" section below). This table, which has been updated for this report from the CDC's website, summarizes number, rate, and type of serious adverse events reported during the period for which data on major adverse event rates and other information were available, both in the Hair loss while taking neurontin U.S. and other countries. Most serious drug reactions are reported from the U.S. A number of serious drug reactions that are reported in other countries described a separate section in the following publication: Riley B, Leffler W, DeGiorgi E. Adverse Events Associated with Antiviral Therapy: Results From the Treatment Clinical Trials Network. Ann Intern Med 2005;142(6):468-72. In the second published report with a serious adverse drug event category (see also "Reporting of Clinical Trials" section below), the following events were reported in the Antiviral Treatment Clinical Trials Network: 

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