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
127567531 12756753 1 I 20160903 20160905 20160917 20160917 EXP BR-SUN PHARMACEUTICAL INDUSTRIES LTD-2016R5-124145 RANBAXY 48.82 YR M Y 60.00000 KG 20160917 CN BR BR

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
127567531 12756753 1 PS CEFUROXIME AXETIL. CEFUROXIME AXETIL 1 Oral 1 DF, BID Y 2732041 0 1 DF TABLET Q12H
127567531 12756753 2 C ATENOLOL. ATENOLOL 1 Oral 25 MG, QD (AT MORNING) U 0 25 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127567531 12756753 1 Testicular disorder
127567531 12756753 2 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127567531 12756753 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127567531 12756753 Blood urine present
127567531 12756753 Confusional state
127567531 12756753 Drug hypersensitivity
127567531 12756753 Pruritus
127567531 12756753 Tachycardia
127567531 12756753 Urinary retention
127567531 12756753 Vision blurred

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
127567531 12756753 1 20160903 20160903 0