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
127864231 12786423 1 I 201403 20160517 20160927 20160927 PER US-FRI-1000084832 ALLERGAN 58.98 YR F Y 0.00000 20160927 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
127864231 12786423 1 PS LINZESS LINACLOTIDE 1 145 ?G, QD Y 202811 145 UG CAPSULE QD
127864231 12786423 2 SS DOXYCYCLINE. DOXYCYCLINE 1 UNK U 0
127864231 12786423 3 SS DOXYCYCLINE. DOXYCYCLINE 1 U 0
127864231 12786423 4 SS CIPROFLOXACIN. CIPROFLOXACIN 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127864231 12786423 1 Irritable bowel syndrome
127864231 12786423 2 Alopecia
127864231 12786423 3 Alopecia
127864231 12786423 4 Urinary tract infection

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127864231 12786423 Alopecia
127864231 12786423 Diarrhoea
127864231 12786423 Erythema
127864231 12786423 Off label use
127864231 12786423 Skin irritation
127864231 12786423 Unevaluable event
127864231 12786423 Urinary tract infection

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
127864231 12786423 1 201403 20160517 0
127864231 12786423 2 2016 0
127864231 12786423 4 2016 0