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
122135494 12213549 4 F 20160215 20160621 20160328 20160712 PER US-PFIZER INC-2016130760 PFIZER 79.00 YR F Y 51.00000 KG 20160712 PH 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
122135494 12213549 1 PS LIPITOR ATORVASTATIN CALCIUM 1 20 MG, UNK Y 20702 20 MG FILM-COATED TABLET
122135494 12213549 2 SS LIPITOR ATORVASTATIN CALCIUM 1 Oral 40 MG, 1X/DAY (BEFORE BEDTIME) Y MI607A 20702 40 MG FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122135494 12213549 1 Blood cholesterol increased
122135494 12213549 2 Hyperlipidaemia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122135494 12213549 Dizziness
122135494 12213549 Gait disturbance
122135494 12213549 Headache
122135494 12213549 Malaise
122135494 12213549 Product taste abnormal
122135494 12213549 Suspected counterfeit product
122135494 12213549 Visual impairment

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
122135494 12213549 2 20160215 20160310 0