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
125821602 12582160 2 F 20160818 20160722 20160831 EXP GB-AUROBINDO-AUR-APL-2016-09052 AUROBINDO 0.00 F Y 0.00000 20160831 OT 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
125821602 12582160 1 PS RAMIPRIL. RAMIPRIL 1 Unknown 5 MG, UNK N U 91604 5 MG
125821602 12582160 2 SS RAMIPRIL. RAMIPRIL 1 Unknown 2.5 MG, UNK N U 91604 2.5 MG
125821602 12582160 3 SS HERCEPTIN TRASTUZUMAB 1 Subcutaneous 600 MG, UNK U U 0 600 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125821602 12582160 1 Product used for unknown indication
125821602 12582160 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125821602 12582160 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125821602 12582160 Blood pressure increased
125821602 12582160 Cough
125821602 12582160 Diarrhoea
125821602 12582160 Influenza
125821602 12582160 Muscle spasms
125821602 12582160 Nail disorder
125821602 12582160 Nasopharyngitis
125821602 12582160 Pyrexia

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

no results found

Therapies reported

no results found