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
93734351 9373435 1 I 20130605 20130624 20130627 20130630 EXP FR-TEVA-415733ISR TEVA 98.92 YR F Y 0.00000 20130630 OT FR FR

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
93734351 9373435 1 PS FUROSEMIDE TEVA 40MG, SCORED TABLET 1 ORAL 40 MILLIGRAM DAILY; D Y175,Y176 18413 40 MG TABLET QD
93734351 9373435 2 SS FUROSEMIDE 1 20 MILLIGRAM DAILY; D 0 20 MG
93734351 9373435 3 C ROCEFIN 1 SUBCUTANEOUS D 0
93734351 9373435 4 C TAMOXIFENE (CITRATE) 2 ORAL 1 DOSAGE FORMS DAILY; D 0 1 DF QD
93734351 9373435 5 C Seretide 1 D 0
93734351 9373435 6 C BRICANYL L.P. 5 mg, sustained release tablet 2 D 0 PROLONGED-RELEASE TABLET
93734351 9373435 7 C Doliprane 1 D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
93734351 9373435 1 Hypertension
93734351 9373435 2 Hypertension
93734351 9373435 3 Bronchitis

Outcome of event

Event ID CASEID OUTC COD
93734351 9373435 DE
93734351 9373435 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
93734351 9373435 Apnoeic attack
93734351 9373435 Death

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
93734351 9373435 1 20130604 20130605 0
93734351 9373435 2 20130604 20130604 0