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
124966042 12496604 2 F 20160604 20160830 20160624 20160906 EXP DE-DRREDDYS-GER/GER/16/0080820 DR REDDYS 57.00 YR M Y 95.00000 KG 20160906 MD DE DE

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
124966042 12496604 1 PS SIMVASTATIN. SIMVASTATIN 1 Oral Y U UNKNOWN 77752 40 MG QD
124966042 12496604 2 C Salbutamol ALBUTEROL 1 Respiratory (inhalation) 2 STROKE IF NECESSARY 0
124966042 12496604 3 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 Respiratory (inhalation) 0 18 UG QD
124966042 12496604 4 C Budiair BUDESONIDE 1 Respiratory (inhalation) 0 200 UG BID
124966042 12496604 5 C Formoterol FORMOTEROL 1 Respiratory (inhalation) 0 1 DF BID
124966042 12496604 6 C Torasemid TORSEMIDE 1 Oral 0 10 MG QD
124966042 12496604 7 C RAMIPRIL. RAMIPRIL 1 Oral 0 5 MG QD
124966042 12496604 8 C ALLOPURINOL. ALLOPURINOL 1 Oral 0 100 MG QD
124966042 12496604 9 C ASPIRIN. ASPIRIN 1 Oral 0 100 MG QD
124966042 12496604 10 C METOPROLOL. METOPROLOL 1 Oral 0 142.5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124966042 12496604 1 Hyperlipidaemia
124966042 12496604 2 Chronic obstructive pulmonary disease
124966042 12496604 3 Chronic obstructive pulmonary disease
124966042 12496604 4 Chronic obstructive pulmonary disease
124966042 12496604 5 Chronic obstructive pulmonary disease
124966042 12496604 6 Cardiac failure
124966042 12496604 7 Hypertension
124966042 12496604 8 Hyperuricaemia
124966042 12496604 9 Product used for unknown indication
124966042 12496604 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124966042 12496604 LT
124966042 12496604 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124966042 12496604 Acute kidney injury
124966042 12496604 Rhabdomyolysis

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found