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

DRUG INTERACTION ( 88 FDA reports)
FALL ( 82 FDA reports)
TREMOR ( 80 FDA reports)
DYSKINESIA ( 76 FDA reports)
DIZZINESS ( 75 FDA reports)
HALLUCINATION ( 69 FDA reports)
PARKINSON'S DISEASE ( 68 FDA reports)
DRUG INEFFECTIVE ( 67 FDA reports)
ANXIETY ( 62 FDA reports)
CONFUSIONAL STATE ( 59 FDA reports)
NAUSEA ( 54 FDA reports)
PATHOLOGICAL GAMBLING ( 54 FDA reports)
SOMNOLENCE ( 54 FDA reports)
DEPRESSION ( 52 FDA reports)
FATIGUE ( 52 FDA reports)
INSOMNIA ( 48 FDA reports)
HEADACHE ( 45 FDA reports)
BLOOD PRESSURE INCREASED ( 44 FDA reports)
PAIN ( 44 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 41 FDA reports)
HYPERSEXUALITY ( 40 FDA reports)
SEROTONIN SYNDROME ( 40 FDA reports)
BALANCE DISORDER ( 38 FDA reports)
GAIT DISTURBANCE ( 37 FDA reports)
MUSCLE SPASMS ( 36 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 32 FDA reports)
EMOTIONAL DISTRESS ( 31 FDA reports)
WEIGHT DECREASED ( 31 FDA reports)
HYPERHIDROSIS ( 30 FDA reports)
MOVEMENT DISORDER ( 30 FDA reports)
PYREXIA ( 30 FDA reports)
SUICIDE ATTEMPT ( 29 FDA reports)
PSYCHOTIC DISORDER ( 28 FDA reports)
TACHYCARDIA ( 28 FDA reports)
HYPERTENSION ( 27 FDA reports)
DIARRHOEA ( 26 FDA reports)
DYSPNOEA ( 26 FDA reports)
ARTHRALGIA ( 25 FDA reports)
DEATH ( 25 FDA reports)
SUICIDAL IDEATION ( 25 FDA reports)
VOMITING ( 25 FDA reports)
ASTHENIA ( 24 FDA reports)
ATRIAL FIBRILLATION ( 24 FDA reports)
FEELING ABNORMAL ( 23 FDA reports)
RESTLESSNESS ( 23 FDA reports)
HYPOTENSION ( 22 FDA reports)
WEIGHT INCREASED ( 22 FDA reports)
ABNORMAL BEHAVIOUR ( 21 FDA reports)
CONDITION AGGRAVATED ( 21 FDA reports)
GAMBLING ( 21 FDA reports)
MAJOR DEPRESSION ( 21 FDA reports)
MUSCULAR WEAKNESS ( 21 FDA reports)
COGNITIVE DISORDER ( 20 FDA reports)
DEHYDRATION ( 20 FDA reports)
ON AND OFF PHENOMENON ( 20 FDA reports)
RENAL FAILURE ( 20 FDA reports)
SYNCOPE ( 20 FDA reports)
PAIN IN EXTREMITY ( 19 FDA reports)
RHABDOMYOLYSIS ( 19 FDA reports)
DECREASED APPETITE ( 18 FDA reports)
PARKINSONISM ( 18 FDA reports)
MALAISE ( 17 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 17 FDA reports)
AGITATION ( 16 FDA reports)
BACK PAIN ( 16 FDA reports)
ECONOMIC PROBLEM ( 16 FDA reports)
HALLUCINATION, VISUAL ( 16 FDA reports)
IMPULSE-CONTROL DISORDER ( 16 FDA reports)
OEDEMA PERIPHERAL ( 16 FDA reports)
CONTUSION ( 15 FDA reports)
DELUSION ( 15 FDA reports)
DRUG EFFECT DECREASED ( 15 FDA reports)
ERYTHEMA ( 15 FDA reports)
HYPOAESTHESIA ( 15 FDA reports)
LIBIDO INCREASED ( 15 FDA reports)
MEMORY IMPAIRMENT ( 15 FDA reports)
OFF LABEL USE ( 15 FDA reports)
RECTAL HAEMORRHAGE ( 15 FDA reports)
AGGRESSION ( 14 FDA reports)
ALOPECIA ( 14 FDA reports)
DYSGRAPHIA ( 14 FDA reports)
INTENTIONAL SELF-INJURY ( 14 FDA reports)
RASH ( 14 FDA reports)
SLEEP DISORDER ( 14 FDA reports)
BLOOD PRESSURE DECREASED ( 13 FDA reports)
CONSTIPATION ( 13 FDA reports)
DISTURBANCE IN ATTENTION ( 13 FDA reports)
DYSSTASIA ( 13 FDA reports)
HIP FRACTURE ( 13 FDA reports)
MYALGIA ( 13 FDA reports)
PANIC ATTACK ( 13 FDA reports)
PARAESTHESIA ( 13 FDA reports)
ABNORMAL DREAMS ( 12 FDA reports)
AMNESIA ( 12 FDA reports)
BLOOD TEST ABNORMAL ( 12 FDA reports)
DELIRIUM ( 12 FDA reports)
HYPERPHAGIA ( 12 FDA reports)
JOINT SWELLING ( 12 FDA reports)
LOSS OF CONSCIOUSNESS ( 12 FDA reports)
MEDICATION ERROR ( 12 FDA reports)
ORTHOSTATIC HYPOTENSION ( 12 FDA reports)
PALPITATIONS ( 12 FDA reports)
PRURITUS ( 12 FDA reports)
URINE COLOUR ABNORMAL ( 12 FDA reports)
VISUAL IMPAIRMENT ( 12 FDA reports)
ABDOMINAL DISCOMFORT ( 11 FDA reports)
APPLICATION SITE PRURITUS ( 11 FDA reports)
CHEST PAIN ( 11 FDA reports)
EPISTAXIS ( 11 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 11 FDA reports)
MUSCLE RIGIDITY ( 11 FDA reports)
PARANOIA ( 11 FDA reports)
SLEEP ATTACKS ( 11 FDA reports)
SUDDEN ONSET OF SLEEP ( 11 FDA reports)
THROMBOCYTOPENIA ( 11 FDA reports)
COMA ( 10 FDA reports)
COMPULSIVE SHOPPING ( 10 FDA reports)
COUGH ( 10 FDA reports)
DRUG ADMINISTRATION ERROR ( 10 FDA reports)
DYSARTHRIA ( 10 FDA reports)
DYSPHAGIA ( 10 FDA reports)
HYPERKALAEMIA ( 10 FDA reports)
MYOCARDIAL INFARCTION ( 10 FDA reports)
NEUTROPENIA ( 10 FDA reports)
NOCTURIA ( 10 FDA reports)
OVERDOSE ( 10 FDA reports)
PNEUMONIA ( 10 FDA reports)
SPEECH DISORDER ( 10 FDA reports)
UNRESPONSIVE TO STIMULI ( 10 FDA reports)
CARDIAC FAILURE ( 9 FDA reports)
DISABILITY ( 9 FDA reports)
FREEZING PHENOMENON ( 9 FDA reports)
HYPERTENSIVE CRISIS ( 9 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 9 FDA reports)
ROAD TRAFFIC ACCIDENT ( 9 FDA reports)
STOMACH DISCOMFORT ( 9 FDA reports)
STRESS ( 9 FDA reports)
TOXIC SKIN ERUPTION ( 9 FDA reports)
URINARY TRACT INFECTION ( 9 FDA reports)
ACCIDENTAL OVERDOSE ( 8 FDA reports)
APPLICATION SITE REACTION ( 8 FDA reports)
ARRHYTHMIA ( 8 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 8 FDA reports)
CONVULSION ( 8 FDA reports)
DRUG DEPENDENCE ( 8 FDA reports)
ERECTILE DYSFUNCTION ( 8 FDA reports)
HYPOTONIA ( 8 FDA reports)
ILL-DEFINED DISORDER ( 8 FDA reports)
INFLUENZA LIKE ILLNESS ( 8 FDA reports)
MOBILITY DECREASED ( 8 FDA reports)
PERSECUTORY DELUSION ( 8 FDA reports)
POOR PERSONAL HYGIENE ( 8 FDA reports)
TENDONITIS ( 8 FDA reports)
VERTIGO ( 8 FDA reports)
COMPLETED SUICIDE ( 7 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 7 FDA reports)
DEPRESSED MOOD ( 7 FDA reports)
DISORIENTATION ( 7 FDA reports)
DRUG DISPENSING ERROR ( 7 FDA reports)
FLUSHING ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
INTENTIONAL OVERDOSE ( 7 FDA reports)
PERSONALITY CHANGE ( 7 FDA reports)
TENDON RUPTURE ( 7 FDA reports)
VASCULITIS ( 7 FDA reports)
VISION BLURRED ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
AKINESIA ( 6 FDA reports)
APPLICATION SITE ERYTHEMA ( 6 FDA reports)
ASTHMA ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
BLOOD URINE PRESENT ( 6 FDA reports)
CEREBROVASCULAR ACCIDENT ( 6 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
DEMENTIA ( 6 FDA reports)
DRUG EFFECT DELAYED ( 6 FDA reports)
FEAR ( 6 FDA reports)
HEAD DISCOMFORT ( 6 FDA reports)
HYPERTHYROIDISM ( 6 FDA reports)
HYPOPHAGIA ( 6 FDA reports)
INJURY ( 6 FDA reports)
MOOD ALTERED ( 6 FDA reports)
NECK PAIN ( 6 FDA reports)
NERVOUSNESS ( 6 FDA reports)
PROSTATE CANCER ( 6 FDA reports)
PSORIASIS ( 6 FDA reports)
THEFT ( 6 FDA reports)
URINARY RETENTION ( 6 FDA reports)
WRIST FRACTURE ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
AKATHISIA ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
BODY TEMPERATURE INCREASED ( 5 FDA reports)
COMPULSIONS ( 5 FDA reports)
DOPAMINE DYSREGULATION SYNDROME ( 5 FDA reports)
DYSTONIA ( 5 FDA reports)
FRUSTRATION ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HALLUCINATION, OLFACTORY ( 5 FDA reports)
INFLAMMATION ( 5 FDA reports)
LEUKOPENIA ( 5 FDA reports)
MEDICATION RESIDUE ( 5 FDA reports)
MENTAL DISORDER ( 5 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 5 FDA reports)
NIGHTMARE ( 5 FDA reports)
PALLOR ( 5 FDA reports)
PRODUCT QUALITY ISSUE ( 5 FDA reports)
RENAL FAILURE CHRONIC ( 5 FDA reports)
RESTLESS LEGS SYNDROME ( 5 FDA reports)
SENSORY LOSS ( 5 FDA reports)
SOPOR ( 5 FDA reports)
THINKING ABNORMAL ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
ADVERSE DRUG REACTION ( 4 FDA reports)
ANAESTHETIC COMPLICATION ( 4 FDA reports)
APPLICATION SITE RASH ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
COLD SWEAT ( 4 FDA reports)
COORDINATION ABNORMAL ( 4 FDA reports)
CORONARY ARTERY DISSECTION ( 4 FDA reports)
CYTOLYTIC HEPATITIS ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DENTAL CARIES ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
EYE DISORDER ( 4 FDA reports)
EYE MOVEMENT DISORDER ( 4 FDA reports)
FACE INJURY ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
HALLUCINATIONS, MIXED ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HYPERTHERMIA ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
HYPOKINESIA ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
IATROGENIC INJURY ( 4 FDA reports)
IMMOBILE ( 4 FDA reports)
INHIBITORY DRUG INTERACTION ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
LEUKOENCEPHALOPATHY ( 4 FDA reports)
LOSS OF CONTROL OF LEGS ( 4 FDA reports)
MANTLE CELL LYMPHOMA ( 4 FDA reports)
MICTURITION URGENCY ( 4 FDA reports)
MIDDLE INSOMNIA ( 4 FDA reports)
MULTIPLE MYELOMA ( 4 FDA reports)
MUSCLE RUPTURE ( 4 FDA reports)
MYOSITIS ( 4 FDA reports)
NEUROPATHY PERIPHERAL ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
OBSESSIVE THOUGHTS ( 4 FDA reports)
ORAL PAIN ( 4 FDA reports)
PAPILLOEDEMA ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PERIRECTAL ABSCESS ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
WEIGHT BEARING DIFFICULTY ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ACCOMMODATION DISORDER ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
APATHY ( 3 FDA reports)
APNOEA ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLADDER DISORDER ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD CHLORIDE INCREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BRACHIAL PLEXOPATHY ( 3 FDA reports)
BRACHIAL PLEXUS INJURY ( 3 FDA reports)
BRADYKINESIA ( 3 FDA reports)
BRADYPHRENIA ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
BURSITIS ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
CORONARY ARTERY STENOSIS ( 3 FDA reports)
DAYDREAMING ( 3 FDA reports)
DECREASED ACTIVITY ( 3 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 3 FDA reports)
DEMENTIA WITH LEWY BODIES ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 3 FDA reports)
DIZZINESS POSTURAL ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
FOAMING AT MOUTH ( 3 FDA reports)
FOOD INTERACTION ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
GROIN PAIN ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
HYPERTONIC BLADDER ( 3 FDA reports)
HYPOGEUSIA ( 3 FDA reports)
IMPAIRED DRIVING ABILITY ( 3 FDA reports)
IMPAIRED SELF-CARE ( 3 FDA reports)
IMPATIENCE ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INFUSION SITE MASS ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
JUDGEMENT IMPAIRED ( 3 FDA reports)
LIMB INJURY ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
LIVEDO RETICULARIS ( 3 FDA reports)
MANIA ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 3 FDA reports)
MUSCLE TWITCHING ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PERFORMANCE STATUS DECREASED ( 3 FDA reports)
PHOTOPHOBIA ( 3 FDA reports)
POLYDIPSIA ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RECTAL CANCER ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
SEXUAL ABUSE ( 3 FDA reports)
SEXUAL DYSFUNCTION ( 3 FDA reports)
SKIN CANCER ( 3 FDA reports)
SKIN INJURY ( 3 FDA reports)
STEREOTYPY ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 3 FDA reports)
TOOTH ABSCESS ( 3 FDA reports)
TOOTH DISORDER ( 3 FDA reports)
TYRAMINE REACTION ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACROCHORDON ( 2 FDA reports)
ALLODYNIA ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
APPLICATION SITE IRRITATION ( 2 FDA reports)
APPLICATION SITE SWELLING ( 2 FDA reports)
APPLICATION SITE URTICARIA ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 2 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 2 FDA reports)
AXONAL NEUROPATHY ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BRAIN DAMAGE ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
BULIMIA NERVOSA ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHEYNE-STOKES RESPIRATION ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CRYING ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
CYST ( 2 FDA reports)
DEPENDENCE ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DISSOCIATIVE FUGUE ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSPHEMIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EJACULATION DISORDER ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOMANIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE NECROSIS ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INJECTION SITE ULCER ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
JAW DISORDER ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LOGORRHOEA ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MORBID THOUGHTS ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PARKINSONIAN GAIT ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POLYARTHRITIS ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PRODUCT COLOUR ISSUE ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PSYCHOLOGICAL TRAUMA ( 2 FDA reports)
PUBIS FRACTURE ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RENAL STONE REMOVAL ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SKIN NEOPLASM EXCISION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 2 FDA reports)
THERAPY REGIMEN CHANGED ( 2 FDA reports)
THOUGHT BLOCKING ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TONGUE HAEMORRHAGE ( 2 FDA reports)
TOOTHACHE ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TRISMUS ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WOUND ( 2 FDA reports)
WRIST SURGERY ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE OEDEMA ( 1 FDA reports)
APPLICATION SITE ULCER ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BINGE EATING ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BISEXUALITY ( 1 FDA reports)
BITE ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE DECREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLLATERAL CIRCULATION ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYCLOTHYMIC DISORDER ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
ERYTHRODERMIC PSORIASIS ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EXCESSIVE SEXUAL FANTASIES ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXHIBITIONISM ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FUMBLING ( 1 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERMETABOLISM ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTHECOSIS ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOINSULINAEMIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
IMMOBILISATION PROLONGED ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INFUSION SITE INFLAMMATION ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
METASTASES TO SKIN ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROMUSCULAR BLOCKADE ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NODULE ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 1 FDA reports)
OCCULT BLOOD NEGATIVE ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARAPHILIA ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PEYRONIE'S DISEASE ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHLEBECTOMY ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PLEUROTHOTONUS ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POST PROCEDURAL HAEMATURIA ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PSEUDOPHAEOCHROMOCYTOMA ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
ROTAVIRUS TEST POSITIVE ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SOMATIC DELUSION ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPINAL HAEMANGIOMA ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUPRANUCLEAR PALSY ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TIC ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULNAR NERVE PALSY ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VARICOSE VEIN OPERATION ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITAMIN D INCREASED ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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