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
126654471 12665447 1 I 20160809 20160818 20160818 EXP CA-ABBVIE-16P-028-1704472-00 ABBVIE 0.00 M Y 91.00000 KG 20160818 CN CA CA

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
126654471 12665447 1 PS BIAXIN CLARITHROMYCIN 1 Unknown U UNKNOWN 50662 1000 MG QD
126654471 12665447 2 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) U UNKNOWN 0 900 MG
126654471 12665447 3 C ALTACE RAMIPRIL 1 0 5 MG QD
126654471 12665447 4 C ASA ASPIRIN 1 0 80 MG QD
126654471 12665447 5 C IMURAN AZATHIOPRINE 1 0 50 MG BID
126654471 12665447 6 C LIPITOR ATORVASTATIN CALCIUM 1 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126654471 12665447 1 Bronchitis
126654471 12665447 2 Colitis ulcerative
126654471 12665447 3 Product used for unknown indication
126654471 12665447 4 Product used for unknown indication
126654471 12665447 5 Product used for unknown indication
126654471 12665447 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126654471 12665447 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126654471 12665447 Bronchitis
126654471 12665447 Erythema
126654471 12665447 Immune thrombocytopenic purpura
126654471 12665447 Pruritus
126654471 12665447 Rotator cuff syndrome
126654471 12665447 Skin reaction

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

no results found

Therapies reported

no results found