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
121110302 12111030 2 F 2016 20160823 20160224 20160831 EXP GB-ABBVIE-16P-167-1567416-00 ABBVIE 44.00 YR M Y 85.00000 KG 20160831 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
121110302 12111030 1 PS CLARITHROMYCIN. CLARITHROMYCIN 1 Oral Y 050164 01/2013 50662 500 MG BID
121110302 12111030 2 C AMOXICILLIN. AMOXICILLIN 1 0
121110302 12111030 3 C DOXYCYCLINE. DOXYCYCLINE 1 0
121110302 12111030 4 C VENTOLIN ALBUTEROL SULFATE 1 Respiratory (inhalation) 0
121110302 12111030 5 C NORMAL SALINE SODIUM CHLORIDE 1 Respiratory (inhalation) 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121110302 12111030 1 Mycoplasma infection
121110302 12111030 2 Product used for unknown indication
121110302 12111030 3 Product used for unknown indication
121110302 12111030 4 Asthma
121110302 12111030 5 Asthma

Outcome of event

Event ID CASEID OUTC COD
121110302 12111030 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121110302 12111030 Amnesia
121110302 12111030 Clumsiness
121110302 12111030 Confusional state
121110302 12111030 Disorganised speech
121110302 12111030 Disturbance in attention
121110302 12111030 Insomnia
121110302 12111030 Jarisch-Herxheimer reaction
121110302 12111030 Liver function test abnormal
121110302 12111030 Restlessness

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
121110302 12111030 1 20160202 0