MedsFacts Reports covering ADDERALL XR (AMPHETAMINE ASPARTATE, AMPHETAMINE SULFATE, DEXTROAMPHETA
Directory listing ordered by most common adverse events for ADDERALL XR (AMPHETAMINE ASPARTATE, AMPHETAMINE SULFATE, DEXTROAMPHETA
Please choose an event type to view the corresponding MedsFacts report:
ABNORMAL BEHAVIOUR ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
OVERDOSE ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
MEDICATION TAMPERING ( 3 FDA reports)
THEFT ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DELUSION ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEAR ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
ANGER ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEDATION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TIC ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
OVERDOSE ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
MEDICATION TAMPERING ( 3 FDA reports)
THEFT ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DELUSION ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEAR ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
ANGER ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEDATION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TIC ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)