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
125484702 12548470 2 F 20160512 20160725 20160712 20160729 EXP IT-ACTAVIS-2016-14498 ACTAVIS 79.19 YR M Y 0.00000 20160729 CN 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
125484702 12548470 1 PS CLOPIDOGREL CLOPIDOGREL BISULFATE 1 Oral UNK Y N UNKNOWN 90307 FILM COATED TABLET
125484702 12548470 2 C MADOPAR BENSERAZIDE HYDROCHLORIDELEVODOPA 1 UNK UNKNOWN 0
125484702 12548470 3 C SIMVASTATIN. SIMVASTATIN 1 Oral 60 MG, DAILY UNKNOWN 0 60 MG TABLETS QD
125484702 12548470 4 C PRITOR PLUS TELMISARTAN 1 UNK UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125484702 12548470 1 Atrial fibrillation
125484702 12548470 2 Product used for unknown indication
125484702 12548470 3 Product used for unknown indication
125484702 12548470 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125484702 12548470 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125484702 12548470 Anaemia
125484702 12548470 Gastric ulcer
125484702 12548470 Melaena

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found