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
127723531 12772353 1 I 20160607 20160914 20160922 20160922 EXP GB-MHRA-EYC 00145051 GB-MYLANLABS-2016M1039719 MYLAN 0.00 Y 0.00000 20160922 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
127723531 12772353 1 PS ATORVASTATIN ATORVASTATIN 1 Oral 10 MG, QD (AT NIGHT) Y U 91226 10 MG QD
127723531 12772353 2 SS FUROSEMIDE. FUROSEMIDE 1 Oral 20 MG, QD (EVERY MORNING) 0 20 MG QD
127723531 12772353 3 SS RAMIPRIL. RAMIPRIL 1 Oral 10 MG, QD (EVERY MORNING) Y U 0 10 MG QD
127723531 12772353 4 C ADCAL D3 CALCIUM CARBONATECHOLECALCIFEROL 1 UNK U 0
127723531 12772353 5 C AMLODIPINE AMLODIPINE BESYLATE 1 UNK U 0
127723531 12772353 6 C ATENOLOL. ATENOLOL 1 UNK U 0
127723531 12772353 7 C BISACODYL. BISACODYL 1 UNK U 0
127723531 12772353 8 C CARMELLOSE 2 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127723531 12772353 1 Hypercholesterolaemia
127723531 12772353 2 Oedema peripheral
127723531 12772353 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127723531 12772353 HO
127723531 12772353 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127723531 12772353 Acute kidney injury
127723531 12772353 Asthenia
127723531 12772353 Dizziness
127723531 12772353 Dyspnoea
127723531 12772353 Fall
127723531 12772353 Hyponatraemia
127723531 12772353 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
127723531 12772353 1 20160609 0