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
125655321 12565532 1 I 20160628 20160706 20160718 20160718 EXP US-BAYER-2016-134690 BAYER 20.00 YR A M Y 0.00000 20160718 CN US 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
125655321 12565532 1 PS ALEVE NAPROXEN SODIUM 1 2 DF, ONCE 20204 2 DF FILM-COATED TABLET 1X
125655321 12565532 2 SS LAMICTAL LAMOTRIGINE 1 Oral 600 MG, QD 0 600 MG QD
125655321 12565532 3 SS LAMICTAL LAMOTRIGINE 1 Oral 100 MG, DAILY 0 100 MG
125655321 12565532 4 C LAMOTRIGINE. LAMOTRIGINE 1 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125655321 12565532 1 Headache
125655321 12565532 2 Epilepsy
125655321 12565532 3 Epilepsy
125655321 12565532 4 Nervous system disorder

Outcome of event

Event ID CASEID OUTC COD
125655321 12565532 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125655321 12565532 Insomnia
125655321 12565532 Salivary hypersecretion
125655321 12565532 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
125655321 12565532 1 20160628 20160628 0
125655321 12565532 3 20111216 0