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
125484802 12548480 2 F 20160728 20160712 20160802 EXP GB-MHRA-EYC 00141466 GB-WATSON-2016-14787 WATSON 77.00 YR F Y 57.15000 KG 20160802 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
125484802 12548480 1 PS RAMIPRIL. RAMIPRIL 1 Oral 2.5 MG, DAILY Y PLO142/0529 76549 2.5 MG CAPSULE, HARD QD
125484802 12548480 2 C CLOPIDOGREL CLOPIDOGREL BISULFATE 1 Unknown UNK U 0
125484802 12548480 3 C ATORVASTATIN ATORVASTATIN 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125484802 12548480 1 Aortic valve replacement
125484802 12548480 2 Product used for unknown indication
125484802 12548480 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125484802 12548480 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125484802 12548480 Nausea
125484802 12548480 Product substitution issue

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
125484802 12548480 1 20160611 20160614 0