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
121887097 12188709 7 F 20160127 20160701 20160317 20160712 EXP GB-ACTAVIS-2016-05873 WATSON 30.00 YR 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
121887097 12188709 1 SS Epirubicin (Unknown) EPIRUBICIN 1 Unknown UNK U UNCONFIRMED 0 UNK
121887097 12188709 2 PS Dexamethasone (Unknown) DEXAMETHASONE 1 Unknown UNK, UNKNOWN U UNCONFIRMED 85456 UNK
121887097 12188709 3 SS Metoclopramide (Unknown) METOCLOPRAMIDE 1 Unknown UNK, UNKNOWN U UNCONFIRMED 0 UNK
121887097 12188709 4 SS Ondansetron (Unknown) ONDANSETRON 1 Unknown UNK, UNKNOWN U UNCONFIRMED 0 UNK
121887097 12188709 5 SS NEULASTA PEGFILGRASTIM 1 Unknown UNK, CYCLE 2 DAY 9, (CYCLICAL) U 0
121887097 12188709 6 SS ZOMETA ZOLEDRONIC ACID 1 Unknown UNK U 0
121887097 12188709 7 SS APREPITANT. APREPITANT 1 Unknown UNK, UNKNOWN U 0
121887097 12188709 8 SS CALCICHEW D3 CALCIUMCHOLECALCIFEROL 1 Unknown UNK, UNKNOWN U 0
121887097 12188709 9 SS LEVOMEPROMAZINE LEVOMEPROMAZINE 1 Unknown UNK, UNKNOWN U 0
121887097 12188709 10 SS TAXOTERE DOCETAXEL 1 Unknown UNK, UNKNOWN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121887097 12188709 1 Product used for unknown indication
121887097 12188709 2 Product used for unknown indication
121887097 12188709 3 Product used for unknown indication
121887097 12188709 4 Product used for unknown indication
121887097 12188709 5 Product used for unknown indication
121887097 12188709 6 Product used for unknown indication
121887097 12188709 7 Product used for unknown indication
121887097 12188709 8 Product used for unknown indication
121887097 12188709 9 Product used for unknown indication
121887097 12188709 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
121887097 12188709 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121887097 12188709 Alopecia
121887097 12188709 Back pain
121887097 12188709 Constipation
121887097 12188709 Dysgeusia
121887097 12188709 Fatigue
121887097 12188709 Neuropathy peripheral
121887097 12188709 Paraesthesia oral
121887097 12188709 Phlebitis
121887097 12188709 Skin discolouration
121887097 12188709 Sunburn

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

no results found

Therapies reported

no results found