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
126845061 12684506 1 I 201604 20160809 20160824 20160824 EXP DE-IBIGEN-2016.02094 IBI LORENZINI 51.00 YR A F Y 97.00000 KG 20160819 CN DE DE

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
126845061 12684506 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 2 DOSAGES 500 MG DAILY DAILY DOSE: 1000 MG MILLGRAM EVERY DAYS N 0 500 MG BID
126845061 12684506 2 SS CLINDAMYCIN CLINDAMYCINCLINDAMYCIN PHOSPHATE 1 Oral DAILY DOSE: 1800 MG MILLGRAM(S) EVERY DAYS 14400 MG N 0 600 MG TID
126845061 12684506 3 SS piperacillin/Tazobactam PIPERACILLIN SODIUMTAZOBACTAM SODIUM 1 Intravenous (not otherwise specified) 3 DOSAGES 4.5 G DAILY DAILY DOSE: 13.5 G GRAM(S) EVERY DAYS N 0 4.5 G TID
126845061 12684506 4 C doxycyclin DOXYCYCLINE 1 Oral DAILY DOSE: 200 MG MILLGRAM(S) EVERY DAYS U 0 200 MG QD
126845061 12684506 5 C tramal long TRAMADOL 1 Oral DAILY DOSE: 200 MG MILLGRAM(S) EVERY DAYS 600 MG U 0 100 MG BID
126845061 12684506 6 C NOVALGIN METAMIZOLE SODIUM 1 Oral DAILY DOSE: 2000 MG MILLGRAM(S) EVERY DAYS 6000 MG U 0 500 MG QID
126845061 12684506 7 C PANTOZOL PANTOPRAZOLE SODIUM 1 Oral DAILY DOSE: 40 MG MILLGRAM(S) EVERY DAYS U 0 40 MG QD
126845061 12684506 8 C mono-embolex CERTOPARIN SODIUM 1 Subcutaneous DAILY DOSE: 3000 IU INTERNATIONAL UNIT(S) EVERY DAYS 9000 IU U 0 3000 IU QD
126845061 12684506 9 C CLINDAMYCIN CLINDAMYCINCLINDAMYCIN PHOSPHATE 1 Oral DAILY DOSE: 1800 MG MILLGRAM(S) EVERY DAYS U 0 600 MG TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126845061 12684506 1 Osteitis
126845061 12684506 2 Osteitis
126845061 12684506 3 Osteitis
126845061 12684506 4 Osteitis
126845061 12684506 5 Pain
126845061 12684506 6 Pain
126845061 12684506 7 Gastritis
126845061 12684506 8 Thrombosis prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126845061 12684506 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126845061 12684506 Epicondylitis
126845061 12684506 Sensory loss
126845061 12684506 Tendon pain

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
126845061 12684506 1 20160402 20160419 0
126845061 12684506 2 20160325 20160402 0
126845061 12684506 3 20160402 20160407 0
126845061 12684506 4 20160408 201605 0
126845061 12684506 5 20160330 20160423 0
126845061 12684506 6 20160330 201605 0
126845061 12684506 7 20160416 20160423 0
126845061 12684506 8 20160330 201605 0
126845061 12684506 9 20160412 20160419 0