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
125432031 12543203 1 I 2014 20160629 20160711 20160711 EXP GB-ACTAVISPR-2016-12820 GB-GLENMARK GENERICS (EUROPE) LTD.-2016GMK023520 GLENMARK 0.00 Y 0.00000 20160711 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
125432031 12543203 1 PS TOPIRAMATE. TOPIRAMATE 1 Oral 25 MG, HS Y 0 25 MG
125432031 12543203 2 SS TOPIRAMATE. TOPIRAMATE 1 Oral 100 MG, BID Y 0 100 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125432031 12543203 1 Essential tremor

Outcome of event

Event ID CASEID OUTC COD
125432031 12543203 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125432031 12543203 Abdominal pain
125432031 12543203 Anal incontinence
125432031 12543203 Cardiovascular disorder
125432031 12543203 Communication disorder
125432031 12543203 Constipation
125432031 12543203 Cough
125432031 12543203 Diarrhoea
125432031 12543203 Dysgraphia
125432031 12543203 Dysphonia
125432031 12543203 Gingival bleeding
125432031 12543203 Hepatic enzyme increased
125432031 12543203 Hypokinesia
125432031 12543203 Joint swelling
125432031 12543203 Palpitations
125432031 12543203 Pancreatic cyst
125432031 12543203 Poor quality sleep
125432031 12543203 Product use issue
125432031 12543203 Pruritus
125432031 12543203 Renal cyst
125432031 12543203 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
125432031 12543203 1 201109 0
125432031 12543203 2 20160204 0