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
7299193 7741087 F 7299193-0 20100101 20110209 20110217 EXP BR-PFIZER INC-2010159599 PFIZERINC 44 YR F Y 72 KG 20110216 CN BRAZIL

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
7299193 1015807215 C METFORMIN 2 UNK
7299193 1015807216 C AMARYL 1 UNK
7299193 1015807210 PS DEPO-PROVERA 1 INTRAMUSCULAR 150 MG, EVERY 3 MONTHS 020246
7299193 1015807211 SS DEPO-PROVERA 1 020246
7299193 1015807212 C HALDOL 1 5 MG, UNK
7299193 1015807213 C AKINETON 1 .5 MG, UNK
7299193 1015807214 C DIAZEPAM 2 10 MG, UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
7299193 1015807215 DIABETES MELLITUS
7299193 1015807216 DIABETES MELLITUS
7299193 1015807210 CONTRACEPTION
7299193 1015807211 MENORRHAGIA
7299193 1015807212 SCHIZOPHRENIA
7299193 1015807214 SLEEP DISORDER

Outcome of event

Event ID OUTC COD
7299193 OT

Reactions reported

Event ID PT
7299193 ARTHROPATHY
7299193 DIABETES MELLITUS INADEQUATE CONTROL
7299193 HYPOAESTHESIA FACIAL
7299193 MENSTRUATION DELAYED
7299193 FINGER DEFORMITY
7299193 WEIGHT DECREASED
7299193 POLLAKIURIA
7299193 FEELING ABNORMAL
7299193 BEDRIDDEN
7299193 OVARIAN CYST
7299193 NERVOUSNESS
7299193 NERVE INJURY
7299193 SYNCOPE
7299193 VAGINAL DISCHARGE
7299193 DIZZINESS
7299193 DROOLING
7299193 MENSTRUAL DISORDER
7299193 TREMOR

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
7299193 1015807215 20050101
7299193 1015807210 20101112
7299193 1015807212 19830101
7299193 1015807213 19830101
7299193 1015807214 19960101