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
125501771 12550177 1 I 20160705 20160712 20160712 EXP GB-ELI_LILLY_AND_COMPANY-GB201607001275 ELI LILLY AND CO 0.00 A F Y 0.00000 20160712 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
125501771 12550177 1 PS Pemetrexed PEMETREXED 1 Unknown UNK UNK, UNKNOWN U U 21462
125501771 12550177 2 SS APREPITANT. APREPITANT 1 Unknown UNK UNK, UNKNOWN U U 0
125501771 12550177 3 SS AVASTIN BEVACIZUMAB 1 Unknown UNK UNK, UNKNOWN U U 0
125501771 12550177 4 SS ENOXAPARIN SODIUM. ENOXAPARIN SODIUM 1 Unknown UNK UNK, UNKNOWN U U 0
125501771 12550177 5 SS XGEVA DENOSUMAB 1 Unknown UNK UNK, UNKNOWN U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125501771 12550177 1 Product used for unknown indication
125501771 12550177 2 Product used for unknown indication
125501771 12550177 3 Product used for unknown indication
125501771 12550177 4 Thrombosis
125501771 12550177 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125501771 12550177 HO
125501771 12550177 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125501771 12550177 Alopecia
125501771 12550177 Blood urine present
125501771 12550177 Constipation
125501771 12550177 Device occlusion
125501771 12550177 Fatigue
125501771 12550177 Haemoglobin decreased
125501771 12550177 Insomnia
125501771 12550177 Pain in extremity

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

no results found

Therapies reported

no results found