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
126629261 12662926 1 I 201606 20160718 20160818 20160818 PER US-STRIDES ARCOLAB LIMITED-2016SP010498 STRIDES 0.00 Y 0.00000 20160818 CN US US

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
126629261 12662926 1 PS TACROLIMUS. TACROLIMUS 1 Oral 1 MG TABLET 6 TIMES A DAY 90687 1 MG
126629261 12662926 2 C MYFORTIC MYCOPHENOLATE SODIUM 1 Oral 180 MG 2 TABLET AT MORNING AND 1 TABLET AT NIGHT 0 180 MG
126629261 12662926 3 C WARFARIN WARFARIN 1 Oral 5 MG -7.5 MG, ONCE DAY 0
126629261 12662926 4 C LEVOTHYROXINE. LEVOTHYROXINE 1 Oral 0.224 MG, QD 0 .224 MG
126629261 12662926 5 C CLARITIN LORATADINE 1 1 DF, PER DAY 0 1 DF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126629261 12662926 1 Immunosuppressant drug therapy
126629261 12662926 2 Immunosuppression
126629261 12662926 3 Coagulopathy
126629261 12662926 4 Hyperthyroidism
126629261 12662926 5 Hypersensitivity

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126629261 12662926 Dizziness
126629261 12662926 Fatigue
126629261 12662926 Headache
126629261 12662926 Hypoaesthesia
126629261 12662926 Memory impairment
126629261 12662926 Muscle spasms
126629261 12662926 Nausea
126629261 12662926 Paraesthesia

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
126629261 12662926 1 201603 0
126629261 12662926 2 200809 0
126629261 12662926 3 1998 0
126629261 12662926 4 2004 0