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
126402551 12640255 1 I 20160525 20160729 20160810 20160810 EXP IT-ACTAVISPR-2016-16798 ACTAVIS 26.18 YR M Y 80.00000 KG 20160810 CN IT IT

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
126402551 12640255 1 PS FINASTERIDE. FINASTERIDE 1 Oral 1 MG, DAILY Y UNKNOWN 77914 1 MG TABLET QD
126402551 12640255 2 SS PROGESTERONE. PROGESTERONE 1 Topical 1 %, CYCLICAL Y UNKNOWN 0 1 PCT
126402551 12640255 3 SS MINOXIDIL. MINOXIDIL 1 Topical 5 %, CYCLICAL Y UNKNOWN 0 5 PCT
126402551 12640255 4 SS 17A-ESTRADIOL ALFATRADIOL 1 Topical 0.025 %, CYCLICAL Y UNKNOWN 0 .025 PCT

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126402551 12640255 1 Androgenetic alopecia
126402551 12640255 2 Androgenetic alopecia
126402551 12640255 3 Androgenetic alopecia
126402551 12640255 4 Androgenetic alopecia

Outcome of event

Event ID CASEID OUTC COD
126402551 12640255 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126402551 12640255 Cerebral infarction
126402551 12640255 Off label use
126402551 12640255 Superior sagittal sinus thrombosis

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
126402551 12640255 2 20151101 20160525 0
126402551 12640255 3 20151101 20160525 0
126402551 12640255 4 20151101 20160525 0