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
127021081 12702108 1 I 201607 20160823 20160831 20160831 EXP FR-009507513-1608FRA013107 MERCK 59.00 YR M Y 0.00000 20160831 CN 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
127021081 12702108 1 PS FIDAXOMICIN FIDAXOMICIN 1 Intravenous (not otherwise specified) UNK Y 201699 TABLET
127021081 12702108 2 SS BACTRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Oral UNK Y 0
127021081 12702108 3 SS MEROPENEM. MEROPENEM 1 Intravenous (not otherwise specified) UNK Y 0
127021081 12702108 4 SS INEXIUM (esomeprazole magnesium) ESOMEPRAZOLE MAGNESIUM 1 Oral UNK Y 0
127021081 12702108 5 C AVODART DUTASTERIDE 1 UNK 0
127021081 12702108 6 C ZARZIO FILGRASTIM 1 UNK 0
127021081 12702108 7 C NOXAFIL POSACONAZOLE 1 Oral UNK 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127021081 12702108 1 Clostridium difficile colitis
127021081 12702108 2 Infection prophylaxis
127021081 12702108 3 Pyrexia

Outcome of event

Event ID CASEID OUTC COD
127021081 12702108 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127021081 12702108 Bone marrow failure
127021081 12702108 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
127021081 12702108 1 20160716 20160726 0
127021081 12702108 2 201607 20160726 0
127021081 12702108 3 20160718 20160802 0
127021081 12702108 4 2016 20160728 0