The Safety Rates Drug Report

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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
126678421 12667842 1 I 20160517 20160531 20160819 20160819 PER US-WATSON-2016-11545 WATSON 64.39 YR F Y 0.00000 20160819 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
126678421 12667842 1 PS CLONIDINE. CLONIDINE 1 Transdermal 0.2 MG, DAILY Y 1077556B 90873 .2 MG TRANSDERMAL PATCH QD
126678421 12667842 2 C ARIMIDEX ANASTROZOLE 1 Oral 1 MG, DAILY UNKNOWN 0 1 MG QD
126678421 12667842 3 C VITAMIN E /00110501/ TOCOPHEROL 1 Unknown UNK, UNKNOWN UNKNOWN 0
126678421 12667842 4 C VITAMIN B12 CYANOCOBALAMIN 1 Unknown UNK, UNKNOWN UNKNOWN 0
126678421 12667842 5 C PROBIOTIC /06395501/ BIFIDOBACTERIUM ANIMALIS SUBSP. LACTIS 1 Unknown UNK, UNKNOWN UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126678421 12667842 1 Hypertension
126678421 12667842 2 Breast cancer
126678421 12667842 3 Product used for unknown indication
126678421 12667842 4 Product used for unknown indication
126678421 12667842 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126678421 12667842 Application site erythema
126678421 12667842 Hallucination
126678421 12667842 Insomnia
126678421 12667842 Restlessness

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
126678421 12667842 1 20160517 20160520 0