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PRODUCT SUBSTITUTION ISSUE ( 20 FDA reports)
ABNORMAL BEHAVIOUR ( 13 FDA reports)
DEPRESSION ( 12 FDA reports)
DRUG INEFFECTIVE ( 12 FDA reports)
HEADACHE ( 10 FDA reports)
ANXIETY ( 9 FDA reports)
DISTURBANCE IN ATTENTION ( 9 FDA reports)
AGITATION ( 8 FDA reports)
ANGER ( 8 FDA reports)
INSOMNIA ( 8 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 8 FDA reports)
AGGRESSION ( 7 FDA reports)
DRUG DISPENSING ERROR ( 7 FDA reports)
MOOD ALTERED ( 7 FDA reports)
FATIGUE ( 6 FDA reports)
SUICIDE ATTEMPT ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
IRRITABILITY ( 5 FDA reports)
RASH ( 5 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
MOOD SWINGS ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
FALL ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
PARANOIA ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
TARDIVE DYSKINESIA ( 3 FDA reports)
THINKING ABNORMAL ( 3 FDA reports)
TIC ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CAT SCRATCH DISEASE ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EXOPHTHALMOS ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
IMPRISONMENT ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MANIA ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PRODUCT COMMINGLING ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
ALCOHOL INTOLERANCE ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATHETOSIS ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BUNION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE INFECTION BACTERIAL ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FIGHT IN SCHOOL ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GROWING PAINS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
MEDICATION TAMPERING ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NAIL PICKING ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHONOLOGICAL DISORDER ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRODUCT LABEL ISSUE ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SEIZURE ANOXIC ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEXUAL ABUSE ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STRESS ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TENSION ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THIRST ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)

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