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

FALL ( 70 FDA reports)
SOMNOLENCE ( 64 FDA reports)
DRUG INEFFECTIVE ( 54 FDA reports)
NAUSEA ( 54 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 44 FDA reports)
DIZZINESS ( 43 FDA reports)
CONDITION AGGRAVATED ( 29 FDA reports)
DYSSTASIA ( 28 FDA reports)
HALLUCINATION ( 28 FDA reports)
ASTHENIA ( 25 FDA reports)
BLOOD PRESSURE INCREASED ( 24 FDA reports)
BLOOD PRESSURE DECREASED ( 21 FDA reports)
HYPERHIDROSIS ( 20 FDA reports)
VOMITING ( 20 FDA reports)
DYSPNOEA ( 19 FDA reports)
HYPOTENSION ( 19 FDA reports)
OEDEMA PERIPHERAL ( 19 FDA reports)
HEADACHE ( 17 FDA reports)
PARANOIA ( 16 FDA reports)
DEATH ( 15 FDA reports)
DRUG EFFECT DECREASED ( 15 FDA reports)
LOSS OF CONSCIOUSNESS ( 15 FDA reports)
DYSKINESIA ( 14 FDA reports)
INJECTION SITE BRUISING ( 14 FDA reports)
FEELING ABNORMAL ( 13 FDA reports)
ABASIA ( 12 FDA reports)
FATIGUE ( 12 FDA reports)
GAIT DISTURBANCE ( 12 FDA reports)
HALLUCINATION, VISUAL ( 12 FDA reports)
AGGRESSION ( 11 FDA reports)
MUSCLE RIGIDITY ( 11 FDA reports)
SPINAL FRACTURE ( 11 FDA reports)
TREMOR ( 11 FDA reports)
URINARY TRACT INFECTION ( 11 FDA reports)
CHEST PAIN ( 10 FDA reports)
MALAISE ( 10 FDA reports)
UNRESPONSIVE TO STIMULI ( 10 FDA reports)
VISION BLURRED ( 10 FDA reports)
CEREBROVASCULAR ACCIDENT ( 9 FDA reports)
CONFUSIONAL STATE ( 9 FDA reports)
FLUSHING ( 9 FDA reports)
MYOCARDIAL INFARCTION ( 9 FDA reports)
PAIN ( 9 FDA reports)
PAIN IN EXTREMITY ( 9 FDA reports)
ARTHRITIS ( 8 FDA reports)
COUGH ( 8 FDA reports)
DYSGEUSIA ( 8 FDA reports)
HIP FRACTURE ( 8 FDA reports)
NERVE COMPRESSION ( 8 FDA reports)
NO THERAPEUTIC RESPONSE ( 8 FDA reports)
PALLOR ( 8 FDA reports)
PNEUMONIA ( 8 FDA reports)
SPINAL COLUMN STENOSIS ( 8 FDA reports)
ABNORMAL BEHAVIOUR ( 7 FDA reports)
ANXIETY ( 7 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 7 FDA reports)
CONTUSION ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
PARKINSON'S DISEASE ( 7 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
IMMOBILE ( 6 FDA reports)
LETHARGY ( 6 FDA reports)
MOVEMENT DISORDER ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
HALLUCINATIONS, MIXED ( 5 FDA reports)
HEAD INJURY ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
INFECTION ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
LIMB DISCOMFORT ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
PANIC ATTACK ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
RHINORRHOEA ( 5 FDA reports)
ARTHRALGIA ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
DEPRESSED MOOD ( 4 FDA reports)
DROOLING ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
FACIAL BONES FRACTURE ( 4 FDA reports)
FREEZING PHENOMENON ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
RESTLESS LEGS SYNDROME ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
YAWNING ( 4 FDA reports)
AMNESIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BRACHIAL PLEXUS INJURY ( 3 FDA reports)
CEREBRAL ATROPHY ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
INJECTION SITE PRURITUS ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
LOWER LIMB FRACTURE ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RETINAL DETACHMENT ( 3 FDA reports)
RIB FRACTURE ( 3 FDA reports)
SENSATION OF PRESSURE ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
UPPER LIMB FRACTURE ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
ANURIA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 2 FDA reports)
DEEP BRAIN STIMULATION ( 2 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC INFECTION BACTERIAL ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LABILE BLOOD PRESSURE ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POSTURE ABNORMAL ( 2 FDA reports)
PULMONARY THROMBOSIS ( 2 FDA reports)
RASH ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SLEEP WALKING ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 2 FDA reports)
THIRST ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
TONGUE DRY ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
URINARY TRACT DISORDER ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
COLON OPERATION ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEMENTIA OF THE ALZHEIMER'S TYPE, WITH DELIRIUM ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FEAR ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IMMEDIATE POST-INJECTION REACTION ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
IMPULSE-CONTROL DISORDER ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INFUSION SITE NECROSIS ( 1 FDA reports)
INFUSION SITE ULCER ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRAOCULAR LENS IMPLANT ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBDURAL HYGROMA ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
URETHRAL PERFORATION ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VOYEURISM ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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