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
121008752 12100875 2 F 20160203 20160823 20160222 20160830 EXP GB-MHRA-EYC 00134958 PHHY2016GB021030 SANDOZ 44.00 YR M Y 85.00000 KG 20160830 OT 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
121008752 12100875 1 PS CLARITHROMYCIN. CLARITHROMYCIN 1 Oral 500 MG, BID 1000 MG Y U 050164 01/2013 65136 500 MG BID
121008752 12100875 2 C AMOXICILLIN. AMOXICILLIN 1 Unknown U 0
121008752 12100875 3 C DOXYCYCLINE. DOXYCYCLINE 1 Unknown UNK U 0
121008752 12100875 4 C VENTOLIN ALBUTEROL SULFATE 1 Respiratory (inhalation) U 0
121008752 12100875 5 C NORMAL SALINE SODIUM CHLORIDE 1 Respiratory (inhalation) U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121008752 12100875 1 Mycoplasma infection
121008752 12100875 2 Product used for unknown indication
121008752 12100875 3 Product used for unknown indication
121008752 12100875 4 Asthma
121008752 12100875 5 Asthma

Outcome of event

Event ID CASEID OUTC COD
121008752 12100875 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121008752 12100875 Amnesia
121008752 12100875 Clumsiness
121008752 12100875 Confusional state
121008752 12100875 Disorganised speech
121008752 12100875 Disturbance in attention
121008752 12100875 Insomnia
121008752 12100875 Jarisch-Herxheimer reaction
121008752 12100875 Liver function test abnormal
121008752 12100875 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
121008752 12100875 1 20160202 0