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
123403292 12340329 2 F 20160726 20160506 20160729 EXP GB-MHRA-EYC 00138430 GB-GLENMARK PHARMACEUTICALS INC, USA.-2016GMK022697 GLENMARK 0.00 Y 0.00000 20160729 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
123403292 12340329 1 PS TOPIRAMATE. TOPIRAMATE 1 Oral 25 MG, UNK Y 77627 25 MG
123403292 12340329 2 SS TOPIRAMATE. TOPIRAMATE 1 100 MG, UNK Y 77627 100 MG
123403292 12340329 3 SS TOPIRAMATE. TOPIRAMATE 1 25 MG, UNK Y 77627 25 MG
123403292 12340329 4 C ANADIN PARACETAMOL ACETAMINOPHEN 1 UNK 0
123403292 12340329 5 C IBUPROFEN. IBUPROFEN 1 UNK 0
123403292 12340329 6 C MIRTAZAPINE. MIRTAZAPINE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123403292 12340329 1 Product used for unknown indication
123403292 12340329 4 Product used for unknown indication
123403292 12340329 5 Product used for unknown indication
123403292 12340329 6 Depression

Outcome of event

Event ID CASEID OUTC COD
123403292 12340329 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123403292 12340329 Headache
123403292 12340329 Hot flush
123403292 12340329 Paraesthesia
123403292 12340329 Seizure

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
123403292 12340329 1 20160307 0
123403292 12340329 3 20160406 0
123403292 12340329 6 2016 0