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
126228171 12622817 1 I 20160610 20160804 20160804 PER GXBR2016US002063 SANDOZ 0.00 M Y 95.24000 KG 20160804 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
126228171 12622817 1 PS TACROLIMUS. TACROLIMUS 1 Topical 1 %, BID U FX2286 200744 1 PCT CREAM BID
126228171 12622817 2 C LISINOPRIL. LISINOPRIL 1 Oral 10 MG, UNK 0 10 MG
126228171 12622817 3 C HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 Oral 200 MG, UNK 0 200 MG
126228171 12622817 4 C SIMVASTATIN. SIMVASTATIN 1 Oral 40 MG, UNK 0 40 MG
126228171 12622817 5 C TRIAMCINOLONE TRIAMCINOLONE 1 UNK DF, UNK 0
126228171 12622817 6 C ACYCLOVIR. ACYCLOVIR 1 UNK DF, UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126228171 12622817 1 Lichen planus
126228171 12622817 2 Hypertension
126228171 12622817 3 Lichen planus
126228171 12622817 4 Blood cholesterol increased
126228171 12622817 5 Lichen planus
126228171 12622817 6 Oral pain

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126228171 12622817 Dysgeusia
126228171 12622817 Incorrect route of drug administration
126228171 12622817 Off label use

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found