About
About Us
Team
Mission
Blog
Drug Search
Tools
Complex Withdrawal
Drug Checklist
Guides & Papers
Post-SSRI Sexual Dysfunction
PSSD Doctors & Specialists
Too Many Drugs?
Glossary
Prize
Side Effect?
Adverse Event Report
Field-by-field reference
Report
reporttype
1
receiptdateformat
102
companynumb
US-PFIZER INC-2014073408
occurcountry
US
Version of Safety Report ID
1
receivedateformat
102
duplicate
1
transmissiondateformat
102
fulfillexpeditecriteria
2
Safety Report ID
10013086
Date Received
14/03/2014
transmissiondate
02/10/2014
serious
2
Date Last Updated
14/03/2014
primarysourcecountry
US
Receiver
receivertype
6
receiverorganization
FDA
Primary Source
reportercountry
US
qualification
1
Sender
sendertype
2
senderorganization
FDA-Public Use
Patient
Onset Age
44
Unit of Onset Age
years
Weight
88.44
Sex
Female
Contents
Reaction
1)
Drug
1)
openFDA Info on Medication
2)
openFDA Info on Medication
Reaction
1)
reactionmeddraversionpt
17.0
Reaction
Drug ineffective
Outcome
Unknown
Drug
1)
drugcharacterization
1
medicinalproduct
ZOLOFT
drugauthorizationnumb
019839
drugstructuredosagenumb
200
drugstructuredosageunit
003
drugseparatedosagenumb
1
drugintervaldosageunitnumb
1
drugintervaldosagedefinition
804
drugdosagetext
200 MG, 1X/DAY
drugindication
PANIC ATTACK
drugstartdateformat
602
drugstartdate
//2002
drugenddateformat
610
drugenddate
/08/2013
actiondrug
1
openFDA Info on Medication
Application Number
NDA020990, NDA019839
Brand Name
ZOLOFT
Generic Name
SERTRALINE HYDROCHLORIDE
Manufacturers
Roerig
product_ndc
0049-0050, 0049-4960, 0049-4900, 0049-4910
Product Type
HUMAN PRESCRIPTION DRUG
Route
ORAL
Active Ingredients
SERTRALINE HYDROCHLORIDE
RXCUI
208149, 208161, 212233, 312938, 312940, 312941, 861064, 861066
spl_id
665a145d-44fb-4fef-a3c1-2aac26e0715c
spl_set_id
fe9e8b7d-61ea-409d-84aa-3ebd79a046b5
Package NDC
0049-4960-30, 0049-4960-50, 0049-4900-30, 0049-4900-66, 0049-4900-73, 0049-4900- ...
Show All
UNII
UTI8907Y6X
2)
drugcharacterization
1
medicinalproduct
ZOLOFT
drugauthorizationnumb
019839
drugindication
ANXIETY
actiondrug
1
openFDA Info on Medication
Application Number
NDA020990, NDA019839
Brand Name
ZOLOFT
Generic Name
SERTRALINE HYDROCHLORIDE
Manufacturers
Roerig
product_ndc
0049-0050, 0049-4960, 0049-4900, 0049-4910
Product Type
HUMAN PRESCRIPTION DRUG
Route
ORAL
Active Ingredients
SERTRALINE HYDROCHLORIDE
RXCUI
208149, 208161, 212233, 312938, 312940, 312941, 861064, 861066
spl_id
665a145d-44fb-4fef-a3c1-2aac26e0715c
spl_set_id
fe9e8b7d-61ea-409d-84aa-3ebd79a046b5
Package NDC
0049-4960-30, 0049-4960-50, 0049-4900-30, 0049-4900-66, 0049-4900-73, 0049-4900- ...
Show All
UNII
UTI8907Y6X
Report Duplicate
duplicatesource
PFIZER
duplicatenumb
US-PFIZER INC-2014073408
Media
Media contact
News releases
Videos
Newsletter
Subscribe to newsletter
Newsletter archive
Follow us
Connect with us
Donate
Contact us