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
125967211 12596721 1 I 20160623 20160715 20160727 20160727 EXP GB-MHRA-EYC 00142279 GB-TEVA-678327ACC TEVA 74.00 YR F Y 0.00000 20160727 PH GB GB

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
125967211 12596721 1 PS ATORVASTATIN ATORVASTATIN 1 Oral 40 MILLIGRAM DAILY; N U 78773 40 MG QD
125967211 12596721 2 C AMLODIPINE AMLODIPINE BESYLATE 1 0
125967211 12596721 3 C CANDESARTAN CANDESARTAN 1 0
125967211 12596721 4 C LANSOPRAZOLE. LANSOPRAZOLE 1 0
125967211 12596721 5 C LEVOTHYROXINE. LEVOTHYROXINE 1 0
125967211 12596721 6 C PARACETAMOL ACETAMINOPHEN 1 0
125967211 12596721 7 C TRAMADOL. TRAMADOL 1 0
125967211 12596721 8 C BETAMETHASONE. BETAMETHASONE 1 0 OINTMENT

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125967211 12596721 DS
125967211 12596721 OT
125967211 12596721 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125967211 12596721 Acute kidney injury
125967211 12596721 Jaundice
125967211 12596721 Malaise
125967211 12596721 Muscular weakness
125967211 12596721 Renal impairment
125967211 12596721 Rhabdomyolysis

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
125967211 12596721 1 20160624 0