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
125368701 12536870 1 I 2014 20160629 20160707 20160707 EXP GB-JNJFOC-20160627148 JANSSEN 85.00 YR E F Y 0.00000 20160707 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
125368701 12536870 1 SS TOPIRAMATE. TOPIRAMATE 1 Oral AT NIGHT Y U UNKNOWN 0 25 MG TABLETS QD
125368701 12536870 2 PS TOPIRAMATE. TOPIRAMATE 1 Oral Y U UNKNOWN 20505 100 MG TABLETS BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125368701 12536870 1 Essential tremor
125368701 12536870 2 Essential tremor

Outcome of event

Event ID CASEID OUTC COD
125368701 12536870 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125368701 12536870 Abdominal pain
125368701 12536870 Anal incontinence
125368701 12536870 Cardiovascular disorder
125368701 12536870 Choking sensation
125368701 12536870 Communication disorder
125368701 12536870 Constipation
125368701 12536870 Cough
125368701 12536870 Diarrhoea
125368701 12536870 Dysgraphia
125368701 12536870 Dysphonia
125368701 12536870 Gingival bleeding
125368701 12536870 Hepatic enzyme increased
125368701 12536870 Hypokinesia
125368701 12536870 Joint swelling
125368701 12536870 Palpitations
125368701 12536870 Pancreatic cyst
125368701 12536870 Poor quality sleep
125368701 12536870 Pruritus
125368701 12536870 Renal cyst
125368701 12536870 Urinary incontinence

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
125368701 12536870 1 201109 0
125368701 12536870 2 20160204 0