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
126102281 12610228 1 I 20160612 20160721 20160801 20160801 EXP GB-MHRA-EYC 00142574 GB-MYLANLABS-2016M1030378 MYLAN 0.00 Y 0.00000 20160801 CN GB GB

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
126102281 12610228 1 PS ISOTRETINOIN ISOTRETINOIN 1 Oral 60 MG, UNK U U 75945 60 MG
126102281 12610228 2 C LYMECYCLINE LYMECYCLINE 1 UNK U 0
126102281 12610228 3 C RIGEVIDON /00022701/ ETHINYL ESTRADIOLLEVONORGESTREL 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126102281 12610228 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126102281 12610228 Alopecia
126102281 12610228 Chapped lips
126102281 12610228 Dry eye
126102281 12610228 Haemorrhoids
126102281 12610228 Oral herpes
126102281 12610228 Pruritus

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
126102281 12610228 1 20160610 0