The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
8248786 8483711 F 8248786-2 20110901 20120321 20120331 EXP US-ALLERGAN-1203596US ALLERGANFDA 39 YR F Y 20120331 CN UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
8248786 1019282888 SS LATISSE 1 70542 022369
8248786 1019282889 C VISINE /00256502/ 2 OPHTHALMIC 2 GTT, PRN
8248786 1019282887 PS LATISSE 1 TOPICAL 2 GTT, QHS FOR ONE AND ONE HALF YEARS 70542 022369
8248786 1019282890 C VISINE /00256502/ 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
8248786 1019282889 DRY EYE
8248786 1019282887 GROWTH OF EYELASHES
8248786 1019282890 ERYTHEMA

Outcome of event

Event ID OUTC COD
8248786 OT

Reactions reported

Event ID PT
8248786 FAECES DISCOLOURED
8248786 NAUSEA
8248786 HEADACHE
8248786 STILLBIRTH
8248786 TRICHORRHEXIS
8248786 OCULAR HYPERAEMIA
8248786 DECREASED APPETITE
8248786 MUCOUS STOOLS
8248786 WRONG TECHNIQUE IN DRUG USAGE PROCESS
8248786 MATERNAL EXPOSURE DURING PREGNANCY
8248786 PRURITUS
8248786 DIARRHOEA HAEMORRHAGIC
8248786 EYE PRURITUS
8248786 ERYTHEMA
8248786 EYE PAIN

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
8248786 1019282889 20110401
8248786 1019282887 20100101 20111001