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
127673531 12767353 1 I 20160803 20160804 20160921 20160921 EXP US-TEVA-685429USA TEVA 29.00 YR F Y 0.00000 20160921 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
127673531 12767353 1 PS AZITHROMYCIN ANHYDROUS. AZITHROMYCIN ANHYDROUS 1 U 73016 65150 TABLET

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127673531 12767353 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127673531 12767353 Abdominal pain upper
127673531 12767353 Anxiety
127673531 12767353 Back pain
127673531 12767353 Chills
127673531 12767353 Diarrhoea
127673531 12767353 Dizziness
127673531 12767353 Dry mouth
127673531 12767353 Feeling hot
127673531 12767353 Insomnia
127673531 12767353 Lip dry
127673531 12767353 Malaise
127673531 12767353 Muscle tightness
127673531 12767353 Myalgia
127673531 12767353 Nasopharyngitis
127673531 12767353 Paraesthesia

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
127673531 12767353 1 20160803 0