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
126136552 12613655 2 F 20151222 20160907 20160802 20160928 EXP GB-DEXPHARM-20161616 DEXCEL 70.00 YR E F Y 0.00000 20160928 OT 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
126136552 12613655 1 PS LANSOPRAZOLE. LANSOPRAZOLE 1 Oral DAILY DOSE: 1 DF DOSAGE FORM EVERY DAYS 741 DF D U 0 1 DF QD
126136552 12613655 2 SS LEVOTHYROXINE. LEVOTHYROXINE 1 Oral DAILY DOSE: 125 ?G MICROGRAM(S) EVERY DAYS 92625 UG D U 0 125 UG QD
126136552 12613655 3 SS SIMVASTATIN. SIMVASTATIN 1 Oral DAILY DOSE: 1 DF DOSAGE FORM EVERY DAYS 564 DF D U 0 1 DF QD
126136552 12613655 4 SS TAMOXIFEN TAMOXIFEN 1 Oral DAILY DOSE: 1 DF DOSAGE FORM EVERY DAYS 2 DF Y U 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126136552 12613655 1 Hiatus hernia
126136552 12613655 2 Hypothyroidism
126136552 12613655 3 Hypercholesterolaemia
126136552 12613655 4 Neoplasm prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126136552 12613655 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126136552 12613655 Anal incontinence
126136552 12613655 Balance disorder
126136552 12613655 Cold sweat
126136552 12613655 Deafness
126136552 12613655 Headache
126136552 12613655 Photosensitivity reaction
126136552 12613655 Vomiting

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
126136552 12613655 1 20131212 0
126136552 12613655 2 20131212 0
126136552 12613655 3 20140607 0
126136552 12613655 4 20151221 20160331 0