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
126300174 12630017 4 F 2016 20160914 20160808 20160928 EXP FR-MALLINCKRODT-T201603405 MALLINCKRODT 10.03 YR M Y 32.00000 KG 20160928 CN US 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
126300174 12630017 1 PS OFIRMEV ACETAMINOPHEN 1 Intravenous (not otherwise specified) UNKNOWN DOSE/FREQUENCY U U UNKNOWN 22450 INJECTION
126300174 12630017 2 SS DOLIPRANE ACETAMINOPHEN 1 Oral UNK UNKNOWN 0
126300174 12630017 3 SS AUGMENTIN AMOXICILLINCLAVULANATE POTASSIUM 1 Intravenous (not otherwise specified) FOR THREE DAYS UNKNOWN 0
126300174 12630017 4 SS CIFLOX CIPROFLOXACIN 1 Intravenous (not otherwise specified) UNK UNKNOWN 0
126300174 12630017 5 SS TAZOCILLINE PIPERACILLIN SODIUMTAZOBACTAM SODIUM 1 Intravenous (not otherwise specified) UNK UNKNOWN 0
126300174 12630017 6 SS FORTUM CEFTAZIDIME 1 Intravenous (not otherwise specified) UNK UNKNOWN 0
126300174 12630017 7 SS FORTUM CEFTAZIDIME 1 Intravenous (not otherwise specified) UNK UNKNOWN 0
126300174 12630017 8 SS ADVIL IBUPROFEN 1 Unknown UNK UNKNOWN 0
126300174 12630017 9 SS REMICADE INFLIXIMAB 1 Unknown UNK U UNKNOWN 0
126300174 12630017 10 SS ZECLAR CLARITHROMYCIN 1 Unknown UNK U 0
126300174 12630017 11 SS VANCOMYCINE VANCOMYCIN 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126300174 12630017 1 Product used for unknown indication
126300174 12630017 2 Product used for unknown indication
126300174 12630017 3 Product used for unknown indication
126300174 12630017 4 Product used for unknown indication
126300174 12630017 5 Product used for unknown indication
126300174 12630017 6 Product used for unknown indication
126300174 12630017 8 Product used for unknown indication
126300174 12630017 9 Product used for unknown indication
126300174 12630017 10 Product used for unknown indication
126300174 12630017 11 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126300174 12630017 HO
126300174 12630017 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126300174 12630017 Cell death
126300174 12630017 Cholestasis
126300174 12630017 Device occlusion
126300174 12630017 Encephalitis
126300174 12630017 Eosinophilia
126300174 12630017 Hepatitis
126300174 12630017 Hyperbilirubinaemia
126300174 12630017 Prothrombin time shortened
126300174 12630017 Toxic epidermal necrolysis

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
126300174 12630017 1 20160626 20160630 0
126300174 12630017 2 20160624 20160625 0
126300174 12630017 3 20160626 20160628 0
126300174 12630017 4 20160627 20160703 0
126300174 12630017 5 20160629 20160703 0
126300174 12630017 6 20160710 20160715 0
126300174 12630017 7 20160717 20160718 0
126300174 12630017 9 20160628 0
126300174 12630017 10 20160701 20160711 0
126300174 12630017 11 20160707 20160725 0