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
125478811 12547881 1 I 20160607 20160712 20160712 EXP US-AUROBINDO-AUR-APL-2016-08039 AUROBINDO 39.00 YR F Y 0.00000 20160712 MD 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
125478811 12547881 1 PS OMEPRAZOLE. OMEPRAZOLE 1 Unknown UNK Y U 203270
125478811 12547881 2 C MELOXICAM. MELOXICAM 1 Unknown UNK Y U 0
125478811 12547881 3 C TRAMADOL. TRAMADOL 1 U 0
125478811 12547881 4 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 U 0
125478811 12547881 5 C RABEPRAZOLE RABEPRAZOLE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125478811 12547881 1 Product used for unknown indication
125478811 12547881 2 Product used for unknown indication
125478811 12547881 3 Product used for unknown indication
125478811 12547881 4 Product used for unknown indication
125478811 12547881 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125478811 12547881 HO
125478811 12547881 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125478811 12547881 Acute kidney injury
125478811 12547881 Asthenia
125478811 12547881 Dysgeusia
125478811 12547881 Dyspnoea exertional
125478811 12547881 Nausea
125478811 12547881 Somnolence
125478811 12547881 Thirst
125478811 12547881 Tubulointerstitial nephritis

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

no results found

Therapies reported

no results found