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
124549793 12454979 3 F 20160329 20160627 20160610 20160705 PER US-PFIZER INC-2016286420 PFIZER 71.00 YR M Y 86.00000 KG 20160705 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
124549793 12454979 1 PS LIPITOR ATORVASTATIN CALCIUM 1 Oral 10 MG, 1X/DAY Y 20702 10 MG FILM-COATED TABLET QD
124549793 12454979 2 SS LIPITOR ATORVASTATIN CALCIUM 1 Y 20702 FILM-COATED TABLET
124549793 12454979 3 SS ATORVASTATIN CALCIUM. ATORVASTATIN CALCIUM 1 Oral 10 MG, 1X/DAY Y M26606 20702 10 MG FILM-COATED TABLET QD
124549793 12454979 4 C OMEPRAZOLE. OMEPRAZOLE 1 20 MG, UNK 0 20 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124549793 12454979 1 Blood cholesterol
124549793 12454979 2 Hyperlipidaemia
124549793 12454979 3 Blood cholesterol
124549793 12454979 4 Gastrooesophageal reflux disease

Outcome of event

Event ID CASEID OUTC COD
124549793 12454979 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124549793 12454979 Blood creatine phosphokinase increased
124549793 12454979 Joint stiffness
124549793 12454979 Movement disorder
124549793 12454979 Muscular weakness
124549793 12454979 Myopathy
124549793 12454979 Product quality issue

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
124549793 12454979 3 20160329 20160426 0