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
127177721 12717772 1 I 20160602 20160829 20160906 20160906 EXP GB-MHRA-EYC 00144298 GB-MYLANLABS-2016M1037035 MYLAN 0.00 Y 0.00000 20160906 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
127177721 12717772 1 PS DOXYCYCLINE. DOXYCYCLINE 1 UNK (500) Y U 62337
127177721 12717772 2 SS ERYTHROMYCIN. ERYTHROMYCIN 1 Oral 250 MG, UNK Y U 0 250 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127177721 12717772 1 Tooth infection
127177721 12717772 2 Tooth infection

Outcome of event

Event ID CASEID OUTC COD
127177721 12717772 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127177721 12717772 Abdominal discomfort
127177721 12717772 Dizziness
127177721 12717772 Facial pain
127177721 12717772 Head discomfort
127177721 12717772 Headache
127177721 12717772 Hyperhidrosis
127177721 12717772 Pyrexia
127177721 12717772 Renal pain

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
127177721 12717772 1 20160816 20160819 0
127177721 12717772 2 20160601 20160606 0