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
127013541 12701354 1 I 201607 20160822 20160831 20160831 EXP FR-ASTRAZENECA-2016SE90861 ASTRAZENECA 59.00 YR M Y 0.00000 20160831 MD 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
127013541 12701354 1 PS INEXIUM ESOMEPRAZOLE 1 Oral Y 21153
127013541 12701354 2 SS MEROPENEM. MEROPENEM 1 Intravenous (not otherwise specified) MYLAN (NON AZ PRODUCT) Y U 0
127013541 12701354 3 SS DIFICLIR FIDAXOMICIN 1 Intravenous (not otherwise specified) Y U 0
127013541 12701354 4 SS BACTRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Oral Y U 0
127013541 12701354 5 C AVODART DUTASTERIDE 1 0
127013541 12701354 6 C ZARZIO FILGRASTIM 1 0
127013541 12701354 7 C NOXAFIL POSACONAZOLE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127013541 12701354 2 Pyrexia
127013541 12701354 3 Clostridium difficile colitis
127013541 12701354 4 Infection prophylaxis

Outcome of event

Event ID CASEID OUTC COD
127013541 12701354 OT
127013541 12701354 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127013541 12701354 Bone marrow failure
127013541 12701354 Clostridium difficile colitis
127013541 12701354 Condition aggravated

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
127013541 12701354 1 2016 20160728 0
127013541 12701354 2 20160718 20160802 0
127013541 12701354 3 20160716 20160726 0
127013541 12701354 4 201607 20160726 0