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FDA AERS Mefloquine, Judicial Watch FOIA report~20120403
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Overdose<br />
Dysgeusia<br />
Hypertension<br />
Oedema<br />
Disturbance In Attention<br />
Visual Field Defect<br />
Paraesthesia<br />
Vomiting<br />
03-Apr-2012 09:37 AM Page: 15
Overdose Dysgeusia Hypertension Oedema Disturbance In Attention Visual Field Defect Paraesthesia Vomiting 03-Apr-2012 09:37 AM Page: 15
<strong>FDA</strong> - Adverse Event Reporting System (<strong>AERS</strong>) Freedom Of Information (FOI) Report Dizziness Report Source Product Role Manufacturer Route Dose Duration Consumer Lariam PS ORAL 250.000 MG Health 1.0 X PER DAY Professional ORAL Date:02/09/98ISR Number: 3025971-XReport Type:Expedited (15-DaCompany Report #88651 Age:28 YR Gender:Female I/FU:I Outcome PT Report Source Product Role Manufacturer Route Dose Duration Other Serious Diplopia Foreign Lariam PS ORAL 250.0000 MG Vith Nerve Paralysis Health 1.0 X PER Nausea Professional WEEK ORAL Headache TAB Date:02/09/98ISR Number: 3026005-3Report Type:Expedited (15-DaCompany Report #93517 Age:73 YR Gender:Male I/FU:I Outcome PT Report Source Product Role Manufacturer Route Dose Duration Life-Threatening Heart Rate Decreased Foreign Lariam PS ORAL 250.0000 MG Hospitalization - Atrioventricular Block Other 1.0 X PER Initial or Prolonged Complete WEEK ORAL Required Dizziness Intervention to Pallor Prevent Permanent Impairment/Damage Date:02/10/98ISR Number: 3027135-2Report Type:Expedited (15-DaCompany Report #87481 Age:53 YR Gender:Male I/FU:F Outcome PT Report Source Product Role Manufacturer Route Dose Duration Disability Mental Impairment Health Lariam PS ORAL 250.000 MG Medication Error Professional 2.0 X WEEK Visual Impairment Other ORAL Vomiting Overdose Hypertension Drug Level Above Therapeutic Dysgeusia Dizziness Brain Injury Visual Acuity Reduced Amnesia Fatigue Paraesthesia Nausea Oedema
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