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
125656921 12565692 1 I 20151222 20160707 20160718 20160718 EXP CN-PFIZER INC-2016343522 PFIZER 78.00 YR M Y 65.00000 KG 20160718 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
125656921 12565692 1 PS LIPITOR ATORVASTATIN CALCIUM 1 Oral 20 MG, 1X/DAY Y M38765 20702 20 MG FILM-COATED TABLET QD
125656921 12565692 2 SS ACETYLSALICYLIC ACID ENTERIC COATED ASPIRIN 1 Oral 300 MG, 1X/DAY Y BJ24792 0 300 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125656921 12565692 1 Cerebral infarction
125656921 12565692 2 Cerebral infarction

Outcome of event

Event ID CASEID OUTC COD
125656921 12565692 OT
125656921 12565692 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125656921 12565692 Asthenia
125656921 12565692 Haemoglobin decreased
125656921 12565692 Pain in extremity
125656921 12565692 Upper respiratory tract infection
125656921 12565692 White blood cell count decreased

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
125656921 12565692 1 20151215 20151223 0
125656921 12565692 2 20151215 20151223 0