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
126031321 12603132 1 I 20160701 20160718 20160728 20160728 EXP GB-MHRA-TPP23477130C2158606YC1467986993273 GB-TEVA-678804ACC TEVA 41.00 YR F Y 93.00000 KG 20160728 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
126031321 12603132 1 PS NITROFURANTOIN. NITROFURANTOIN 1 Oral Y U 73652
126031321 12603132 2 C FEMOSTON DYDROGESTERONEESTRADIOL 1 1 DOSAGE FORMS DAILY; 400 DF 0 1 DF QD
126031321 12603132 3 C FLUCONAZOLE. FLUCONAZOLE 1 USE AS DIRECTED 0
126031321 12603132 4 C FLUOXETINE FLUOXETINE HYDROCHLORIDE 1 1 DOSAGE FORMS DAILY; 400 DF 0 1 DF QD

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126031321 12603132 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126031321 12603132 Asthenia
126031321 12603132 Diarrhoea
126031321 12603132 Dizziness
126031321 12603132 Headache
126031321 12603132 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
126031321 12603132 1 20160701 20160708 0
126031321 12603132 2 20150528 0
126031321 12603132 3 20160701 20160708 0
126031321 12603132 4 20150528 20160518 0