The Safety Rates Drug Report

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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
127075631 12707563 1 I 20140312 20160822 20160901 20160901 EXP PHHY2016ES118875 SANDOZ 75.00 YR M Y 0.00000 20160901 OT ES ES

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
127075631 12707563 1 SS SINTROM ACENOCOUMAROL 1 Oral UNK Y 0 TABLET
127075631 12707563 2 PS SIMVASTATINA SIMVASTATIN 1 Oral UNK Y 77766
127075631 12707563 3 SS PENTOXIFILINA PENTOXIFYLLINE 1 Oral UNK Y 0
127075631 12707563 4 C BISOPROLOL BISOPROLOL 1 Oral UNK 0
127075631 12707563 5 C METFORMIN METFORMIN HYDROCHLORIDE 1 Oral UNK Y 0
127075631 12707563 6 C LEVETIRACETAM. LEVETIRACETAM 1 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127075631 12707563 1 Atrial fibrillation
127075631 12707563 2 Hyperlipidaemia
127075631 12707563 3 Pain
127075631 12707563 4 Atrial fibrillation
127075631 12707563 5 Type 2 diabetes mellitus
127075631 12707563 6 Epilepsy

Outcome of event

Event ID CASEID OUTC COD
127075631 12707563 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127075631 12707563 Subdural haematoma

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
127075631 12707563 1 201308 20140312 0
127075631 12707563 2 20140312 0
127075631 12707563 3 20140312 0
127075631 12707563 5 20140319 0
127075631 12707563 6 201308 0