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
102841722 10284172 2 F 20160627 20140708 20160705 PER US-PFIZER INC-2014185137 PFIZER 62.00 YR F Y 61.22000 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
102841722 10284172 1 PS LYRICA PREGABALIN 1 Oral 50 MG, 3X/DAY 21446 50 MG CAPSULE, HARD TID
102841722 10284172 2 SS LYRICA PREGABALIN 1 Oral 100 MG, 3X/DAY 21446 100 MG CAPSULE, HARD TID
102841722 10284172 3 C MELOXICAM. MELOXICAM 1 UNK 0
102841722 10284172 4 C CRESTOR ROSUVASTATIN CALCIUM 1 UNK 0
102841722 10284172 5 C PLAVIX CLOPIDOGREL BISULFATE 1 75 MG, UNK 0 75 MG
102841722 10284172 6 C NORVASC AMLODIPINE BESYLATE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
102841722 10284172 1 Complex regional pain syndrome
102841722 10284172 2 Myofascial pain syndrome
102841722 10284172 3 Arthritis
102841722 10284172 6 Blood pressure abnormal

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
102841722 10284172 Burning sensation
102841722 10284172 Product use 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
102841722 10284172 1 201203 0