The Safety Rates Drug Report

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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
125870851 12587085 1 I 20151029 20151210 20160725 20160725 PER US-PFIZER INC-3114338 PFIZER 62.00 YR M Y 118.80000 KG 20160725 CN US 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
125870851 12587085 1 PS VANCOMYCIN HCL VANCOMYCIN HYDROCHLORIDE 1 UNK Y UNK 62911
125870851 12587085 2 SS INVESTIGATIONAL DRUG INVESTIGATIONAL PRODUCT 1 Subcutaneous FREQ: 1 WEEK; INTERVAL: 2 UNK 0
125870851 12587085 3 SS PLACEBO UNSPECIFIED INGREDIENT 1 Subcutaneous FREQ: 1 WEEK; INTERVAL: 2 UNK 0
125870851 12587085 4 C NOVOLIN INSULIN HUMAN 1 Subcutaneous 16 IU, FREQ: 1 DAY; INTERVAL: 1 0 16 IU
125870851 12587085 5 C NOVOLIN INSULIN HUMAN 1 Subcutaneous 18 IU, FREQ: 1 DAY; INTERVAL: 1 0 18 IU
125870851 12587085 6 C ASPIRIN /00002701/ ASPIRIN 1 Oral 81 MG, FREQ: 1 DAY; INTERVAL: 1 0 81 MG
125870851 12587085 7 C BENAZEPRIL BENAZEPRIL HYDROCHLORIDE 1 Oral 10 MG, FREQ: 1 DAY; INTERVAL: 1 0 10 MG
125870851 12587085 8 C CARVEDILOL. CARVEDILOL 1 Oral 25 MG, FREQ: 2 DAY; INTERVAL: 1 0 25 MG
125870851 12587085 9 C DICLOFENAC DICLOFENAC 1 Topical 1 %, FREQ: AS NECESSARY 0 1 PCT GEL
125870851 12587085 10 C ERYTHROMYCIN. ERYTHROMYCIN 1 DOSE: 1 APP; ROUTE OF ADMINISTRATION: OINT, FREQ: AS NECESSARY 0 OINTMENT
125870851 12587085 11 C SIMVASTATIN. SIMVASTATIN 1 Oral 40 MG, FREQ: 1 DAY; INTERVAL: 1 0 40 MG
125870851 12587085 12 C SPIRONOLACTONE. SPIRONOLACTONE 1 Oral 25 MG, FREQ: AS NECESSARY 0 25 MG
125870851 12587085 13 C WARFARIN WARFARIN 1 Oral 5 MG, X 1 WEEK 0 5 MG
125870851 12587085 14 C WARFARIN WARFARIN 1 Oral 7.5 MG, X 6 WEEK 0 7.5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125870851 12587085 1 Product used for unknown indication
125870851 12587085 2 Cardiovascular disorder
125870851 12587085 3 Cardiovascular disorder
125870851 12587085 4 Diabetes mellitus
125870851 12587085 6 Atrial fibrillation
125870851 12587085 7 Hypertension
125870851 12587085 8 Cardiac failure congestive
125870851 12587085 9 Osteoarthritis
125870851 12587085 10 Blepharitis
125870851 12587085 11 Hyperlipidaemia
125870851 12587085 12 Cardiac failure congestive
125870851 12587085 13 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
125870851 12587085 HO
125870851 12587085 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125870851 12587085 Acute kidney injury
125870851 12587085 Osteomyelitis

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
125870851 12587085 1 20151101 20151101 0
125870851 12587085 2 20141212 20150306 0
125870851 12587085 3 20141212 20150306 0
125870851 12587085 4 20110101 0
125870851 12587085 5 20110101 0
125870851 12587085 6 20040101 0
125870851 12587085 7 20040101 20151128 0
125870851 12587085 8 20110101 0
125870851 12587085 9 20110101 0
125870851 12587085 10 20110101 0
125870851 12587085 11 20080101 0
125870851 12587085 12 20110101 20151128 0
125870851 12587085 13 19950101 0
125870851 12587085 14 19950101 0