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
125487821 12548782 1 I 2014 20160629 20160712 20160712 EXP GB-TEVA-673487ACC TEVA 83.00 YR F Y 0.00000 20160712 CN GB GB

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
125487821 12548782 1 PS TOPIRAMATE. TOPIRAMATE 1 Oral 200 MILLIGRAM DAILY; 200 MG (100 MG, BID) Y U UNKNOWN 76317 100 MG CAPSULE, HARD BID
125487821 12548782 2 SS TOPIRAMATE. TOPIRAMATE 1 Oral 25 MG AT NIGHT Y U UNKNOWN 76317 25 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125487821 12548782 1 Essential tremor

Outcome of event

Event ID CASEID OUTC COD
125487821 12548782 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125487821 12548782 Abdominal pain
125487821 12548782 Anal incontinence
125487821 12548782 Cardiovascular disorder
125487821 12548782 Communication disorder
125487821 12548782 Constipation
125487821 12548782 Cough
125487821 12548782 Diarrhoea
125487821 12548782 Dysgraphia
125487821 12548782 Dysphonia
125487821 12548782 Gingival bleeding
125487821 12548782 Hepatic enzyme increased
125487821 12548782 Hypokinesia
125487821 12548782 Joint swelling
125487821 12548782 Palpitations
125487821 12548782 Pancreatic cyst
125487821 12548782 Poor quality sleep
125487821 12548782 Pruritus
125487821 12548782 Renal cyst
125487821 12548782 Urinary incontinence

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

no results found

Therapies reported

no results found