Language selection

Search

2008-03-25 - Female

300392

Adverse reaction report number 300392
Latest AER version number 0
Market authorization holder AER number N/A
Initial received date 2008-03-25
Latest received date 2008-03-25
Age N/A
Gender Female
Weight N/A
Type of report Spontaneous
Reporter type Pharmacist
Source of report Community
Report outcome Unknown
Serious report? No

Product information

Product description Dosage form Health product role Route of administration Dose Frequency Therapy duration Indication(s)
ADDERALL XRCAPSULE, EXTENDED RELEASESuspectUnknown Attention deficit/hyperactivity disorder

Adverse reaction term information

MedDRA version: v.21.1
Adverse reaction terms Reaction duration
Weight decreased
Date modified: