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
126415321 12641532 1 I 20160421 20160810 20160810 EXP US-PFIZER INC-3276748 PFIZER 66.00 YR F Y 0.00000 20160810 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
126415321 12641532 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 500 MG, FREQ: 2 DAY; INTERVAL: 1 UNK 77245 500 MG
126415321 12641532 2 SS CIPROFLOXACIN. CIPROFLOXACIN 1 500 MG, 2X/DAY 77245 500 MG BID
126415321 12641532 3 SS MELOXICAM. MELOXICAM 1 15 MG, FREQ: 1 DAY; INTERVAL: 1 UNK 0 15 MG
126415321 12641532 4 SS MELOXICAM. MELOXICAM 1 15 MG, DAILY 0 15 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126415321 12641532 1 Urinary tract infection
126415321 12641532 3 Osteoarthritis

Outcome of event

Event ID CASEID OUTC COD
126415321 12641532 OT
126415321 12641532 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126415321 12641532 Acute kidney injury
126415321 12641532 Granulomatosis with polyangiitis
126415321 12641532 Haemorrhage
126415321 12641532 Retroperitoneal haemorrhage
126415321 12641532 Tubulointerstitial nephritis

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

no results found

Therapies reported

no results found