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
126102232 12610223 2 F 20151222 20160916 20160801 20160926 EXP GB-MHRA-EYC 00142519 GB-MYLANLABS-2016M1030251 MYLAN 0.00 Y 0.00000 20160926 MD 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
126102232 12610223 1 PS LANSOPRAZOLE. LANSOPRAZOLE 1 Oral 1 DF, QD (IN THE MORNING.) 740 DF D 90763 1 DF QD
126102232 12610223 2 SS SIMVASTATIN. SIMVASTATIN 1 Oral 1 DF, QD (AT NIGHT.) 563.41992 DF D 0 1 DF QD
126102232 12610223 3 SS TAMOXIFEN TAMOXIFEN 1 Oral 1 DF, QD 1 DF D 0 1 DF QD
126102232 12610223 4 SS LEVOTHYROXINE. LEVOTHYROXINE 1 Oral 125 ?G, QD 92500 UG D 0 125 UG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126102232 12610223 1 Hiatus hernia
126102232 12610223 2 Hypercholesterolaemia
126102232 12610223 3 Neoplasm prophylaxis
126102232 12610223 4 Hypothyroidism

Outcome of event

Event ID CASEID OUTC COD
126102232 12610223 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126102232 12610223 Anal incontinence
126102232 12610223 Balance disorder
126102232 12610223 Cold sweat
126102232 12610223 Deafness
126102232 12610223 Feeling cold
126102232 12610223 Headache
126102232 12610223 Hyperhidrosis
126102232 12610223 Photosensitivity reaction
126102232 12610223 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
126102232 12610223 1 20131212 0
126102232 12610223 2 20140607 0
126102232 12610223 3 20151221 20160331 0
126102232 12610223 4 20131212 0