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
126268182 12626818 2 F 20160525 20160829 20160805 20160901 EXP IT-MINISAL02-369417 IT-MYLANLABS-2016M1031938 MYLAN 0.00 Y 0.00000 20160901 MD 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
126268182 12626818 1 PS FINASTERIDE. FINASTERIDE 1 Oral 1 MG, QD Y 77578 1 MG TABLET QD
126268182 12626818 2 SS PROGESTERONE. PROGESTERONE 1 Topical 1 %, CYCLE Y 0 1 PCT CUTANEOUS SOLUTION
126268182 12626818 3 SS MINOXIDIL. MINOXIDIL 1 Topical 5 %, CYCLE Y 0 5 PCT CUTANEOUS SOLUTION
126268182 12626818 4 SS ALFA-ESTRADIOL ALFATRADIOL 1 Topical UNK Y 0 SOLUTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126268182 12626818 1 Androgenetic alopecia
126268182 12626818 2 Androgenetic alopecia
126268182 12626818 3 Androgenetic alopecia
126268182 12626818 4 Androgenetic alopecia

Outcome of event

Event ID CASEID OUTC COD
126268182 12626818 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126268182 12626818 Cerebral infarction
126268182 12626818 Venous 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
126268182 12626818 2 20151101 20160525 0
126268182 12626818 3 20151101 20160525 0
126268182 12626818 4 20151101 20160525 0