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
126423971 12642397 1 I 20151210 20160802 20160810 20160810 EXP PHHY2016IT108358 SANDOZ 86.73 YR F Y 0.00000 20160810 OT IT IT

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
126423971 12642397 1 PS ACETYLSALICYLIC ACID ASPIRIN 1 Unknown 100 MG, QD 34400 MG 0 100 MG QD
126423971 12642397 2 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown 0 FILM-COATED TABLET
126423971 12642397 3 C TRITTICO TRAZODONE HYDROCHLORIDE 1 Unknown U 0
126423971 12642397 4 C EBIXA MEMANTINE HYDROCHLORIDE 1 Unknown U 0
126423971 12642397 5 C TAVOR (LORAZEPAM) LORAZEPAM 1 Unknown U 0
126423971 12642397 6 C ZYLLT CLOPIDOGREL BISULFATE 1 Unknown U 0
126423971 12642397 7 C LAROXYL AMITRIPTYLINE 1 Unknown U 0
126423971 12642397 8 C LEVOTHYROXINE. LEVOTHYROXINE 1 Unknown U 0
126423971 12642397 9 C RAMIPRIL. RAMIPRIL 1 Unknown U 0
126423971 12642397 10 C RANITIDINE. RANITIDINE 1 Unknown U 0
126423971 12642397 11 C ATORVASTATIN ATORVASTATIN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126423971 12642397 1 Antiplatelet therapy
126423971 12642397 2 Antiplatelet therapy
126423971 12642397 3 Product used for unknown indication
126423971 12642397 4 Product used for unknown indication
126423971 12642397 5 Product used for unknown indication
126423971 12642397 6 Product used for unknown indication
126423971 12642397 7 Product used for unknown indication
126423971 12642397 8 Product used for unknown indication
126423971 12642397 9 Product used for unknown indication
126423971 12642397 10 Product used for unknown indication
126423971 12642397 11 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126423971 12642397 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126423971 12642397 Cerebral haemorrhage

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
126423971 12642397 1 20150101 20151210 0
126423971 12642397 2 20150101 20151210 0