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
125242081 12524208 1 I 201412 20160622 20160704 20160704 EXP GB-DRREDDYS-GER/UKI/16/0080921 DR REDDYS 34.00 YR F Y 72.40000 KG 20160704 CN 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
125242081 12524208 1 PS OLANZAPINE. OLANZAPINE 1 Oral N U UNKNOWN 76133 20 MG TABLET
125242081 12524208 2 SS OLANZAPINE. OLANZAPINE 1 Oral N U UNKNOWN 76133 5 MG TABLET QD
125242081 12524208 3 C TRANEXAMIC ACID. TRANEXAMIC ACID 1 Oral 0 500 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125242081 12524208 1 Schizophrenia
125242081 12524208 3 Menorrhagia

Outcome of event

Event ID CASEID OUTC COD
125242081 12524208 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125242081 12524208 Amenorrhoea
125242081 12524208 Anxiety
125242081 12524208 Hyperprolactinaemia
125242081 12524208 Hypertrichosis
125242081 12524208 Oligomenorrhoea
125242081 12524208 Uterine leiomyoma
125242081 12524208 Weight increased

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
125242081 12524208 1 201412 0
125242081 12524208 2 201412 0
125242081 12524208 3 201512 0