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
126595801 12659580 1 I 20151210 20160810 20160817 20160817 EXP CN-PFIZER INC-2016386724 PFIZER 77.00 YR F Y 52.00000 KG 20160817 OT CN CN

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
126595801 12659580 1 PS LIPITOR ATORVASTATIN CALCIUM 1 Oral 20 MG, 1X/DAY 600 MG Y M30562 20702 20 MG FILM-COATED TABLET QD
126595801 12659580 2 SS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 Intravenous drip 250 ML, 1X/DAY 4500 ML Y 0 250 ML INJECTION QD
126595801 12659580 3 SS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 Intravenous drip 250 ML, 1X/DAY 4500 ML Y BXH6AB3 0 250 ML INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126595801 12659580 1 Lipids abnormal
126595801 12659580 2 Lung disorder

Outcome of event

Event ID CASEID OUTC COD
126595801 12659580 DS
126595801 12659580 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126595801 12659580 Blood creatine phosphokinase MB increased
126595801 12659580 Blood creatine phosphokinase increased
126595801 12659580 Blood creatinine increased

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
126595801 12659580 1 20151111 20151213 0
126595801 12659580 2 20151117 20151125 0
126595801 12659580 3 20151202 20151211 0