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
127692661 12769266 1 I 201606 20160913 20160921 20160921 EXP FR-ABBVIE-16P-056-1734363-00 ABBVIE 9.96 YR M Y 32.00000 KG 20160921 OT FR FR

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
127692661 12769266 1 PS ZECLAR CLARITHROMYCIN 1 Unknown Y UNKNOWN 50662
127692661 12769266 2 SS DOLIPRANE ACETAMINOPHEN 1 Oral Y UNKNOWN 0
127692661 12769266 3 SS PERFALGAN ACETAMINOPHEN 1 Intravenous (not otherwise specified) Y UNKNOWN 0
127692661 12769266 4 SS AUGMENTIN AMOXICILLINCLAVULANATE POTASSIUM 1 Intravenous (not otherwise specified) Y UNKNOWN 0
127692661 12769266 5 SS CIFLOX CIPROFLOXACIN 1 Intravenous (not otherwise specified) Y UNKNOWN 0
127692661 12769266 6 SS TAZOCILLINE PIPERACILLIN SODIUMTAZOBACTAM SODIUM 1 Intravenous (not otherwise specified) Y UNKNOWN 0
127692661 12769266 7 SS REMICADE INFLIXIMAB 1 Unknown Y UNKNOWN 0
127692661 12769266 8 SS FORTUM CEFTAZIDIME 1 Intravenous (not otherwise specified) Y UNKNOWN 0
127692661 12769266 9 SS FORTUM CEFTAZIDIME 1 Intravenous (not otherwise specified) Y UNKNOWN 0
127692661 12769266 10 SS VANCOMYCINE VANCOMYCIN 1 Unknown Y UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127692661 12769266 1 Product used for unknown indication
127692661 12769266 2 Product used for unknown indication
127692661 12769266 3 Product used for unknown indication
127692661 12769266 4 Product used for unknown indication
127692661 12769266 5 Product used for unknown indication
127692661 12769266 6 Product used for unknown indication
127692661 12769266 7 Product used for unknown indication
127692661 12769266 8 Product used for unknown indication
127692661 12769266 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127692661 12769266 LT
127692661 12769266 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127692661 12769266 Cell death
127692661 12769266 Cholestasis
127692661 12769266 Eosinophilia
127692661 12769266 Hyperbilirubinaemia
127692661 12769266 Prothrombin time shortened

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
127692661 12769266 1 20160711 0
127692661 12769266 2 20160624 20160625 0
127692661 12769266 3 20160626 20160630 0
127692661 12769266 4 20160626 20160628 0
127692661 12769266 5 20160627 20160703 0
127692661 12769266 6 20160629 20160703 0
127692661 12769266 7 20160628 20160628 0
127692661 12769266 8 20160710 20160715 0
127692661 12769266 9 20160717 20160718 0
127692661 12769266 10 20160707 20160725 0