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
125631821 12563182 1 I 20160706 20160715 20160715 EXP GB-SA-2016SA125168 AVENTIS 58.00 YR A F Y 0.00000 20160715 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
125631821 12563182 1 PS CLEXANE ENOXAPARIN SODIUM 1 Unknown UNK, UNKNOWN U UNK 20164
125631821 12563182 2 SS AVASTIN BEVACIZUMAB 1 Unknown UNK, UNKNOWN U UNK 0
125631821 12563182 3 SS ALIMTA PEMETREXED DISODIUM 1 Unknown UNK, UNKNOWN U UNK 0 INJECTION
125631821 12563182 4 SS XGEVA DENOSUMAB 1 Unknown UNK, UNKNOWN U UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125631821 12563182 1 Pulmonary thrombosis

Outcome of event

Event ID CASEID OUTC COD
125631821 12563182 HO
125631821 12563182 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125631821 12563182 Alopecia
125631821 12563182 Blood urine present
125631821 12563182 Constipation
125631821 12563182 Fatigue
125631821 12563182 Haemoglobin decreased
125631821 12563182 Obstructive uropathy
125631821 12563182 Pain in extremity
125631821 12563182 Pulmonary embolism
125631821 12563182 Sleep disorder

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

no results found

Therapies reported

no results found