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
125395052 12539505 2 F 20160720 20160708 20160728 EXP US-MLMSERVICE-20160706-0306746-1 US-STRIDES ARCOLAB LIMITED-2016SP009127 STRIDES 0.00 Y 0.00000 20160728 OT GB US

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
125395052 12539505 1 PS METRONIDAZOLE. METRONIDAZOLE 1 UNK 208162
125395052 12539505 2 SS CIPROFLOXACIN. CIPROFLOXACIN 1 UNK 0
125395052 12539505 3 SS LINEZOLID. LINEZOLID 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125395052 12539505 1 Diverticulitis
125395052 12539505 2 Diverticulitis
125395052 12539505 3 Urinary tract infection

Outcome of event

Event ID CASEID OUTC COD
125395052 12539505 HO
125395052 12539505 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125395052 12539505 Abdominal pain
125395052 12539505 Abdominal tenderness
125395052 12539505 Anaemia
125395052 12539505 Bandaemia
125395052 12539505 Blood pressure systolic increased
125395052 12539505 Clostridium difficile colitis
125395052 12539505 Diarrhoea
125395052 12539505 Dysuria
125395052 12539505 Enterovesical fistula
125395052 12539505 Faecaluria
125395052 12539505 Leukocytosis
125395052 12539505 Urinary retention

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

no results found

Therapies reported

no results found