The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126672461 12667246 1 I 20160727 0 20160818 20160818 DIR 57.00 YR F N 135.00000 LBS 20160817 N US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126672461 12667246 1 PS TOPAMAX TOPIRAMATE 1 Oral TOPAMAX - 1 DAILY FOR 5 DAYS - MOUTH N D 0 1 DF
126672461 12667246 3 C CALCIUM CALCIUM 1 0
126672461 12667246 5 C MULTIVITAMIN VITAMINS 1 0
126672461 12667246 7 C COLLAGEN-MSM 2 0
126672461 12667246 9 C ACETAMINOPHEN,CAFFEINE, BUTALBITAL 2 0
126672461 12667246 17 C LIPITOR ATORVASTATIN CALCIUM 1 0
126672461 12667246 19 C AZITHROMYCIN (ZITHROMAX Z-PAK) 2 0
126672461 12667246 21 C BLOOD SUGAR DIAGNOSTIC (ONE TOUCH ULTRA TEST) 2 0
126672461 12667246 23 C CALCIUM CALCIUM 1 0
126672461 12667246 25 C DICYCLOMINE (BENTYL) 2 0
126672461 12667246 27 C DIPHENOXYLATE-ATROPINE (LOMOTIL) 2 0
126672461 12667246 29 C ESTRADIOL (ESTRACE) 2 0
126672461 12667246 31 C EZETIMIBE (ZETIA) 2 0
126672461 12667246 33 C FLUTICASONE (FLONASE) 2 0
126672461 12667246 35 C MOBIC MELOXICAM 1 0
126672461 12667246 37 C MOBIC MELOXICAM 1 0
126672461 12667246 39 C MULTIVITAMIN (DAILY MULTI-VITAMIN) 2 0
126672461 12667246 41 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 0
126672461 12667246 43 C TOPAMAX TOPIRAMATE 1 0
126672461 12667246 45 C ZOLMITRIPTAN (ZOMIG) 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126672461 12667246 1 Migraine

Outcome of event

Event ID CASEID OUTC COD
126672461 12667246 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126672461 12667246 Abdominal distension
126672461 12667246 Abdominal pain upper
126672461 12667246 Arthralgia
126672461 12667246 Asthenia
126672461 12667246 Balance disorder
126672461 12667246 Burning sensation
126672461 12667246 Clumsiness
126672461 12667246 Confusional state
126672461 12667246 Decreased activity
126672461 12667246 Diarrhoea
126672461 12667246 Diplopia
126672461 12667246 Disturbance in attention
126672461 12667246 Dyspnoea
126672461 12667246 Eye irritation
126672461 12667246 Eye pain
126672461 12667246 Fatigue
126672461 12667246 Intraocular pressure increased
126672461 12667246 Myalgia
126672461 12667246 Nervousness
126672461 12667246 Ocular hyperaemia
126672461 12667246 Paraesthesia
126672461 12667246 Respiratory rate increased
126672461 12667246 Somnolence
126672461 12667246 Speech disorder
126672461 12667246 Tinnitus
126672461 12667246 Vision blurred
126672461 12667246 Visual acuity reduced

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126672461 12667246 1 20160727 20160727 0