Please choose an event type to view the corresponding MedsFacts report:

HEADACHE ( 10 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
FATIGUE ( 6 FDA reports)
NAUSEA ( 5 FDA reports)
PRODUCT QUALITY ISSUE ( 5 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 5 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
PAIN ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
AGITATION ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DYSPHEMIA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FEAR ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
MANIA ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
RASH ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TIC ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRISMUS ( 1 FDA reports)

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