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

DEPRESSION ( 315 FDA reports)
NAUSEA ( 294 FDA reports)
FATIGUE ( 291 FDA reports)
DRUG INEFFECTIVE ( 277 FDA reports)
INSOMNIA ( 223 FDA reports)
ANXIETY ( 219 FDA reports)
HEADACHE ( 194 FDA reports)
SOMNOLENCE ( 181 FDA reports)
AGGRESSION ( 178 FDA reports)
PAIN ( 169 FDA reports)
SUICIDAL IDEATION ( 166 FDA reports)
WEIGHT INCREASED ( 164 FDA reports)
DIZZINESS ( 163 FDA reports)
CONVULSION ( 147 FDA reports)
VOMITING ( 137 FDA reports)
DYSPNOEA ( 131 FDA reports)
FEELING ABNORMAL ( 131 FDA reports)
CHEST PAIN ( 122 FDA reports)
ABNORMAL BEHAVIOUR ( 116 FDA reports)
AGITATION ( 104 FDA reports)
ABDOMINAL PAIN UPPER ( 102 FDA reports)
WEIGHT DECREASED ( 101 FDA reports)
DECREASED APPETITE ( 95 FDA reports)
RASH ( 94 FDA reports)
TREMOR ( 92 FDA reports)
HYPERHIDROSIS ( 91 FDA reports)
OEDEMA PERIPHERAL ( 91 FDA reports)
BACK PAIN ( 89 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 88 FDA reports)
DIARRHOEA ( 86 FDA reports)
ARTHRALGIA ( 85 FDA reports)
IRRITABILITY ( 85 FDA reports)
FALL ( 84 FDA reports)
HEART RATE INCREASED ( 83 FDA reports)
PYREXIA ( 83 FDA reports)
ASTHENIA ( 82 FDA reports)
DISTURBANCE IN ATTENTION ( 82 FDA reports)
CONDITION AGGRAVATED ( 81 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 81 FDA reports)
PAIN IN EXTREMITY ( 80 FDA reports)
LOSS OF CONSCIOUSNESS ( 76 FDA reports)
PSYCHOTIC DISORDER ( 75 FDA reports)
PARAESTHESIA ( 71 FDA reports)
MOOD SWINGS ( 70 FDA reports)
CONFUSIONAL STATE ( 69 FDA reports)
OVERDOSE ( 69 FDA reports)
SUICIDE ATTEMPT ( 69 FDA reports)
ABDOMINAL PAIN ( 67 FDA reports)
MALAISE ( 66 FDA reports)
DRUG INTERACTION ( 65 FDA reports)
PALPITATIONS ( 65 FDA reports)
PULMONARY EMBOLISM ( 64 FDA reports)
COUGH ( 62 FDA reports)
HYPERTENSION ( 62 FDA reports)
MUSCLE SPASMS ( 62 FDA reports)
HALLUCINATION ( 61 FDA reports)
HYPOAESTHESIA ( 61 FDA reports)
ALOPECIA ( 60 FDA reports)
VISION BLURRED ( 60 FDA reports)
ANGER ( 59 FDA reports)
CONSTIPATION ( 57 FDA reports)
DYSKINESIA ( 57 FDA reports)
MEMORY IMPAIRMENT ( 57 FDA reports)
AMNESIA ( 56 FDA reports)
GASTROINTESTINAL DISORDER ( 55 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 55 FDA reports)
INJURY ( 54 FDA reports)
PRESCRIBED OVERDOSE ( 54 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 52 FDA reports)
LETHARGY ( 52 FDA reports)
PARANOIA ( 52 FDA reports)
PRURITUS ( 52 FDA reports)
CHOLELITHIASIS ( 50 FDA reports)
CRYING ( 50 FDA reports)
DRUG EFFECT DECREASED ( 50 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 49 FDA reports)
DIABETES MELLITUS ( 49 FDA reports)
CHEST DISCOMFORT ( 48 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 48 FDA reports)
PNEUMONIA ( 47 FDA reports)
ROAD TRAFFIC ACCIDENT ( 47 FDA reports)
BIPOLAR DISORDER ( 46 FDA reports)
MIGRAINE ( 46 FDA reports)
BLOOD PRESSURE INCREASED ( 45 FDA reports)
DEATH ( 45 FDA reports)
GAIT DISTURBANCE ( 45 FDA reports)
TACHYCARDIA ( 44 FDA reports)
THIRST ( 44 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 43 FDA reports)
CROHN'S DISEASE ( 43 FDA reports)
DEEP VEIN THROMBOSIS ( 43 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 43 FDA reports)
URINARY TRACT INFECTION ( 43 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 41 FDA reports)
RECTAL HAEMORRHAGE ( 41 FDA reports)
INTESTINAL HAEMORRHAGE ( 40 FDA reports)
ERYTHEMA ( 39 FDA reports)
CONTUSION ( 38 FDA reports)
DEHYDRATION ( 38 FDA reports)
MYALGIA ( 38 FDA reports)
TIC ( 38 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 38 FDA reports)
CHOLECYSTITIS CHRONIC ( 35 FDA reports)
MULTI-ORGAN DISORDER ( 35 FDA reports)
PANIC ATTACK ( 35 FDA reports)
SINUSITIS ( 35 FDA reports)
TARDIVE DYSKINESIA ( 35 FDA reports)
BITE ( 34 FDA reports)
COLITIS ( 34 FDA reports)
DRY MOUTH ( 34 FDA reports)
EMOTIONAL DISORDER ( 34 FDA reports)
ILL-DEFINED DISORDER ( 34 FDA reports)
URTICARIA ( 34 FDA reports)
ANOREXIA ( 33 FDA reports)
DYSPEPSIA ( 33 FDA reports)
INFLUENZA LIKE ILLNESS ( 33 FDA reports)
INTENTIONAL OVERDOSE ( 33 FDA reports)
SYNCOPE ( 33 FDA reports)
ARTHRITIS ( 32 FDA reports)
COGNITIVE DISORDER ( 32 FDA reports)
MANIA ( 32 FDA reports)
NASOPHARYNGITIS ( 32 FDA reports)
CARDIOMEGALY ( 31 FDA reports)
CHILLS ( 31 FDA reports)
COMPULSIONS ( 31 FDA reports)
DRUG DOSE OMISSION ( 31 FDA reports)
DRY SKIN ( 31 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 31 FDA reports)
ASTHMA ( 30 FDA reports)
DYSPHAGIA ( 30 FDA reports)
INCORRECT DOSE ADMINISTERED ( 30 FDA reports)
NERVOUSNESS ( 30 FDA reports)
OFF LABEL USE ( 30 FDA reports)
TREATMENT NONCOMPLIANCE ( 30 FDA reports)
ABDOMINAL DISCOMFORT ( 29 FDA reports)
ANAEMIA ( 29 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 29 FDA reports)
COMPLETED SUICIDE ( 29 FDA reports)
DRUG SCREEN POSITIVE ( 29 FDA reports)
INTENTIONAL DRUG MISUSE ( 29 FDA reports)
PRODUCT QUALITY ISSUE ( 29 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 28 FDA reports)
DELUSION ( 28 FDA reports)
SLEEP DISORDER ( 28 FDA reports)
ABDOMINAL DISTENSION ( 27 FDA reports)
ABNORMAL DREAMS ( 27 FDA reports)
CELLULITIS ( 27 FDA reports)
COLITIS ULCERATIVE ( 27 FDA reports)
DRUG TOXICITY ( 27 FDA reports)
DYSTONIA ( 27 FDA reports)
HAEMORRHOIDS ( 27 FDA reports)
HEPATIC ENZYME INCREASED ( 27 FDA reports)
NIGHTMARE ( 27 FDA reports)
SKIN DISCOLOURATION ( 27 FDA reports)
THINKING ABNORMAL ( 27 FDA reports)
UNEVALUABLE EVENT ( 27 FDA reports)
APATHY ( 26 FDA reports)
DYSPNOEA EXERTIONAL ( 26 FDA reports)
IMPULSIVE BEHAVIOUR ( 26 FDA reports)
STAPHYLOCOCCAL INFECTION ( 26 FDA reports)
DRUG ABUSER ( 25 FDA reports)
DRUG DEPENDENCE ( 25 FDA reports)
FLUSHING ( 25 FDA reports)
HOMICIDAL IDEATION ( 25 FDA reports)
HOT FLUSH ( 25 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 25 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 25 FDA reports)
THROMBOSIS ( 25 FDA reports)
HALLUCINATION, VISUAL ( 24 FDA reports)
HYPERGLYCAEMIA ( 24 FDA reports)
MENTAL DISORDER ( 24 FDA reports)
MULTIPLE SCLEROSIS ( 24 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 24 FDA reports)
MUSCLE TWITCHING ( 24 FDA reports)
BLOOD GLUCOSE INCREASED ( 23 FDA reports)
BLOOD PRESSURE DECREASED ( 23 FDA reports)
HYPOTENSION ( 23 FDA reports)
SEDATION ( 23 FDA reports)
STEVENS-JOHNSON SYNDROME ( 23 FDA reports)
VISUAL IMPAIRMENT ( 23 FDA reports)
BONE PAIN ( 22 FDA reports)
DEPRESSED MOOD ( 22 FDA reports)
HALLUCINATION, AUDITORY ( 22 FDA reports)
MUSCULAR WEAKNESS ( 22 FDA reports)
MUSCULOSKELETAL PAIN ( 22 FDA reports)
NECK PAIN ( 22 FDA reports)
PANCREATITIS ( 22 FDA reports)
PREGNANCY ( 22 FDA reports)
RESTLESSNESS ( 22 FDA reports)
WITHDRAWAL SYNDROME ( 22 FDA reports)
DRY EYE ( 21 FDA reports)
FEELING HOT ( 21 FDA reports)
GRAND MAL CONVULSION ( 21 FDA reports)
HYPERSENSITIVITY ( 21 FDA reports)
MOOD ALTERED ( 21 FDA reports)
RENAL FAILURE ( 21 FDA reports)
SELF MUTILATION ( 21 FDA reports)
VISUAL ACUITY REDUCED ( 21 FDA reports)
WHEEZING ( 21 FDA reports)
ACCIDENTAL OVERDOSE ( 20 FDA reports)
BLISTER ( 20 FDA reports)
CARDIAC DISORDER ( 20 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 20 FDA reports)
DELIRIUM ( 20 FDA reports)
DYSGEUSIA ( 20 FDA reports)
JOINT SWELLING ( 20 FDA reports)
NARCOLEPSY ( 20 FDA reports)
SPEECH DISORDER ( 20 FDA reports)
STRESS ( 20 FDA reports)
TINNITUS ( 20 FDA reports)
ATELECTASIS ( 19 FDA reports)
COMA ( 19 FDA reports)
GALLBLADDER DISORDER ( 19 FDA reports)
INJECTION SITE PAIN ( 19 FDA reports)
POLLAKIURIA ( 19 FDA reports)
PULMONARY HYPERTENSION ( 19 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 19 FDA reports)
BALANCE DISORDER ( 18 FDA reports)
CEREBROVASCULAR ACCIDENT ( 18 FDA reports)
CHROMATURIA ( 18 FDA reports)
FOLLICULITIS ( 18 FDA reports)
HEPATIC STEATOSIS ( 18 FDA reports)
LIMB DISCOMFORT ( 18 FDA reports)
LYMPHADENOPATHY ( 18 FDA reports)
MEDICATION ERROR ( 18 FDA reports)
MULTI-ORGAN FAILURE ( 18 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 18 FDA reports)
PERSONALITY CHANGE ( 18 FDA reports)
RESPIRATORY DISTRESS ( 18 FDA reports)
SKIN EXFOLIATION ( 18 FDA reports)
STOMACH DISCOMFORT ( 18 FDA reports)
AFFECT LABILITY ( 17 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 17 FDA reports)
COORDINATION ABNORMAL ( 17 FDA reports)
DISORIENTATION ( 17 FDA reports)
DYSARTHRIA ( 17 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 17 FDA reports)
FEAR ( 17 FDA reports)
HAEMATOCHEZIA ( 17 FDA reports)
HYPERSOMNIA ( 17 FDA reports)
IMPAIRED WORK ABILITY ( 17 FDA reports)
INTENTIONAL SELF-INJURY ( 17 FDA reports)
IRRITABLE BOWEL SYNDROME ( 17 FDA reports)
LIP DRY ( 17 FDA reports)
MENSTRUATION IRREGULAR ( 17 FDA reports)
NEUROPATHY PERIPHERAL ( 17 FDA reports)
OSTEOPENIA ( 17 FDA reports)
PALLOR ( 17 FDA reports)
SCAR ( 17 FDA reports)
SEROTONIN SYNDROME ( 17 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 17 FDA reports)
TYPE 1 DIABETES MELLITUS ( 17 FDA reports)
TYPE 2 DIABETES MELLITUS ( 17 FDA reports)
VERTIGO ( 17 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 17 FDA reports)
DILATATION VENTRICULAR ( 16 FDA reports)
FAECAL INCONTINENCE ( 16 FDA reports)
HALLUCINATIONS, MIXED ( 16 FDA reports)
INCREASED APPETITE ( 16 FDA reports)
MYOCARDIAL INFARCTION ( 16 FDA reports)
PLEURAL EFFUSION ( 16 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 16 FDA reports)
RASH PRURITIC ( 16 FDA reports)
RESPIRATORY FAILURE ( 16 FDA reports)
URINARY INCONTINENCE ( 16 FDA reports)
ABORTION SPONTANEOUS ( 15 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 15 FDA reports)
ARTHROPATHY ( 15 FDA reports)
CARDIOPULMONARY FAILURE ( 15 FDA reports)
EAR PAIN ( 15 FDA reports)
EMOTIONAL DISTRESS ( 15 FDA reports)
FLATULENCE ( 15 FDA reports)
HEAD INJURY ( 15 FDA reports)
IMPAIRED DRIVING ABILITY ( 15 FDA reports)
NASAL CONGESTION ( 15 FDA reports)
NEPHROLITHIASIS ( 15 FDA reports)
RENAL FAILURE ACUTE ( 15 FDA reports)
SKIN LACERATION ( 15 FDA reports)
SWELLING ( 15 FDA reports)
ANAL FISTULA ( 14 FDA reports)
ARRHYTHMIA ( 14 FDA reports)
CARDIOMYOPATHY ( 14 FDA reports)
DIPLOPIA ( 14 FDA reports)
DIVERTICULUM ( 14 FDA reports)
DRUG HYPERSENSITIVITY ( 14 FDA reports)
ERECTILE DYSFUNCTION ( 14 FDA reports)
GASTRITIS ( 14 FDA reports)
HEART RATE DECREASED ( 14 FDA reports)
MYDRIASIS ( 14 FDA reports)
OSTEOARTHRITIS ( 14 FDA reports)
PLATELET COUNT INCREASED ( 14 FDA reports)
SKIN LESION ( 14 FDA reports)
UNRESPONSIVE TO STIMULI ( 14 FDA reports)
ANHEDONIA ( 13 FDA reports)
ATRIAL SEPTAL DEFECT ( 13 FDA reports)
CARDIAC ARREST ( 13 FDA reports)
CHOLECYSTECTOMY ( 13 FDA reports)
CONCUSSION ( 13 FDA reports)
DRUG DISPENSING ERROR ( 13 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 13 FDA reports)
FUNGAL SKIN INFECTION ( 13 FDA reports)
HAEMATOCRIT DECREASED ( 13 FDA reports)
INJECTION SITE ERYTHEMA ( 13 FDA reports)
LABORATORY TEST ABNORMAL ( 13 FDA reports)
MAJOR DEPRESSION ( 13 FDA reports)
MOVEMENT DISORDER ( 13 FDA reports)
OROPHARYNGEAL PAIN ( 13 FDA reports)
PERICARDIAL EFFUSION ( 13 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 13 FDA reports)
RASH GENERALISED ( 13 FDA reports)
SENSORY DISTURBANCE ( 13 FDA reports)
SINUS TACHYCARDIA ( 13 FDA reports)
SPINAL OSTEOARTHRITIS ( 13 FDA reports)
TENDONITIS ( 13 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 13 FDA reports)
ALCOHOL USE ( 12 FDA reports)
APHASIA ( 12 FDA reports)
BLINDNESS ( 12 FDA reports)
BLOOD IRON DECREASED ( 12 FDA reports)
BLOOD URINE PRESENT ( 12 FDA reports)
BRONCHITIS ( 12 FDA reports)
BURNING SENSATION ( 12 FDA reports)
CARPAL TUNNEL SYNDROME ( 12 FDA reports)
COLD SWEAT ( 12 FDA reports)
ERUCTATION ( 12 FDA reports)
EXCORIATION ( 12 FDA reports)
EYE PAIN ( 12 FDA reports)
FOAMING AT MOUTH ( 12 FDA reports)
HEART RATE IRREGULAR ( 12 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 12 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 12 FDA reports)
MITRAL VALVE INCOMPETENCE ( 12 FDA reports)
MUSCLE TIGHTNESS ( 12 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 12 FDA reports)
PERIRECTAL ABSCESS ( 12 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 12 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 12 FDA reports)
RHABDOMYOLYSIS ( 12 FDA reports)
SWELLING FACE ( 12 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 12 FDA reports)
UNINTENDED PREGNANCY ( 12 FDA reports)
ABASIA ( 11 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 11 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 11 FDA reports)
CYST ( 11 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 11 FDA reports)
DRUG ABUSE ( 11 FDA reports)
DRUG ADMINISTRATION ERROR ( 11 FDA reports)
DRUG DIVERSION ( 11 FDA reports)
ECONOMIC PROBLEM ( 11 FDA reports)
EPISTAXIS ( 11 FDA reports)
GASTRIC DISORDER ( 11 FDA reports)
HAEMATEMESIS ( 11 FDA reports)
HEPATITIS C ( 11 FDA reports)
HOSTILITY ( 11 FDA reports)
HYPOAESTHESIA ORAL ( 11 FDA reports)
HYPOVOLAEMIA ( 11 FDA reports)
ILEITIS ( 11 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 11 FDA reports)
LOGORRHOEA ( 11 FDA reports)
LYMPHADENITIS ( 11 FDA reports)
MENORRHAGIA ( 11 FDA reports)
MULTIPLE DRUG OVERDOSE ( 11 FDA reports)
MUSCLE ATROPHY ( 11 FDA reports)
NIGHT SWEATS ( 11 FDA reports)
OEDEMA ( 11 FDA reports)
OSTEOPOROSIS ( 11 FDA reports)
PELVIC FRACTURE ( 11 FDA reports)
PNEUMOTHORAX ( 11 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 11 FDA reports)
RESPIRATORY ARREST ( 11 FDA reports)
SINUS BRADYCARDIA ( 11 FDA reports)
SKIN BACTERIAL INFECTION ( 11 FDA reports)
TOOTH DISORDER ( 11 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 11 FDA reports)
BRONCHOPLEURAL FISTULA ( 10 FDA reports)
CAROTIDYNIA ( 10 FDA reports)
CHRONIC FATIGUE SYNDROME ( 10 FDA reports)
CYANOSIS ( 10 FDA reports)
DIABETIC KETOACIDOSIS ( 10 FDA reports)
DYSMENORRHOEA ( 10 FDA reports)
DYSPHEMIA ( 10 FDA reports)
DYSSTASIA ( 10 FDA reports)
ECZEMA ( 10 FDA reports)
EMPHYSEMA ( 10 FDA reports)
FLUID RETENTION ( 10 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 10 FDA reports)
GLAUCOMA ( 10 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 10 FDA reports)
HYPOAESTHESIA FACIAL ( 10 FDA reports)
LIPOHYPERTROPHY ( 10 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 10 FDA reports)
MENTAL IMPAIRMENT ( 10 FDA reports)
MENTAL STATUS CHANGES ( 10 FDA reports)
METABOLIC ACIDOSIS ( 10 FDA reports)
NASAL DRYNESS ( 10 FDA reports)
NERVOUS SYSTEM DISORDER ( 10 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 10 FDA reports)
PAIN IN JAW ( 10 FDA reports)
PAPILLOEDEMA ( 10 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 10 FDA reports)
PROCTITIS ULCERATIVE ( 10 FDA reports)
RASH ERYTHEMATOUS ( 10 FDA reports)
RETCHING ( 10 FDA reports)
SCOLIOSIS ( 10 FDA reports)
SPINAL COLUMN INJURY ( 10 FDA reports)
SPINAL FRACTURE ( 10 FDA reports)
SUICIDAL BEHAVIOUR ( 10 FDA reports)
TOOTH FRACTURE ( 10 FDA reports)
ACNE ( 9 FDA reports)
AUTISM ( 9 FDA reports)
BILIARY COLIC ( 9 FDA reports)
BLOOD GLUCOSE DECREASED ( 9 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 9 FDA reports)
CERVICAL SPINAL STENOSIS ( 9 FDA reports)
CLOSTRIDIAL INFECTION ( 9 FDA reports)
DENTAL CARIES ( 9 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 9 FDA reports)
DRUG TOLERANCE ( 9 FDA reports)
DYSPHONIA ( 9 FDA reports)
EAR INFECTION ( 9 FDA reports)
EXPIRED DRUG ADMINISTERED ( 9 FDA reports)
EYE ROLLING ( 9 FDA reports)
GALLBLADDER INJURY ( 9 FDA reports)
HAEMOGLOBIN DECREASED ( 9 FDA reports)
HAEMORRHAGE ( 9 FDA reports)
HYPOXIA ( 9 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 9 FDA reports)
INITIAL INSOMNIA ( 9 FDA reports)
INJECTION SITE HAEMORRHAGE ( 9 FDA reports)
INTENTIONAL MISUSE ( 9 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 9 FDA reports)
LIBIDO DECREASED ( 9 FDA reports)
MEDICATION RESIDUE ( 9 FDA reports)
MOBILITY DECREASED ( 9 FDA reports)
MUSCLE SPASTICITY ( 9 FDA reports)
NEUTROPHIL COUNT INCREASED ( 9 FDA reports)
OBESITY ( 9 FDA reports)
OSTEONECROSIS OF JAW ( 9 FDA reports)
PERSONALITY DISORDER ( 9 FDA reports)
POOR QUALITY SLEEP ( 9 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 9 FDA reports)
RAYNAUD'S PHENOMENON ( 9 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 9 FDA reports)
RHEUMATOID ARTHRITIS ( 9 FDA reports)
RHINITIS ( 9 FDA reports)
RHINORRHOEA ( 9 FDA reports)
ROTATOR CUFF SYNDROME ( 9 FDA reports)
SCREAMING ( 9 FDA reports)
STARING ( 9 FDA reports)
SWOLLEN TONGUE ( 9 FDA reports)
SYNOVIAL CYST ( 9 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 9 FDA reports)
THORACIC OUTLET SYNDROME ( 9 FDA reports)
THYROID DISORDER ( 9 FDA reports)
VISUAL DISTURBANCE ( 9 FDA reports)
ABSCESS ( 8 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 8 FDA reports)
ADVERSE DRUG REACTION ( 8 FDA reports)
ADVERSE EVENT ( 8 FDA reports)
AKATHISIA ( 8 FDA reports)
AMENORRHOEA ( 8 FDA reports)
ANGINA PECTORIS ( 8 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 8 FDA reports)
AORTA HYPOPLASIA ( 8 FDA reports)
AORTIC VALVE INCOMPETENCE ( 8 FDA reports)
APNOEA ( 8 FDA reports)
ASPIRATION ( 8 FDA reports)
BICUSPID AORTIC VALVE ( 8 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 8 FDA reports)
BREAST CANCER ( 8 FDA reports)
BRUXISM ( 8 FDA reports)
CARDIOVASCULAR DISORDER ( 8 FDA reports)
COARCTATION OF THE AORTA ( 8 FDA reports)
COMMUNICATION DISORDER ( 8 FDA reports)
DEAFNESS ( 8 FDA reports)
DISCOMFORT ( 8 FDA reports)
DISSOCIATION ( 8 FDA reports)
DROOLING ( 8 FDA reports)
DYSGRAPHIA ( 8 FDA reports)
DYSURIA ( 8 FDA reports)
EDUCATIONAL PROBLEM ( 8 FDA reports)
FEELING COLD ( 8 FDA reports)
FEELING JITTERY ( 8 FDA reports)
FOOT FRACTURE ( 8 FDA reports)
FUNGAL INFECTION ( 8 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 8 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
HEPATITIS ( 8 FDA reports)
HUMERUS FRACTURE ( 8 FDA reports)
HYPERTENSIVE CRISIS ( 8 FDA reports)
HYPERVENTILATION ( 8 FDA reports)
HYPOPLASTIC RIGHT HEART SYNDROME ( 8 FDA reports)
INFECTION ( 8 FDA reports)
INFLUENZA ( 8 FDA reports)
JOINT EFFUSION ( 8 FDA reports)
KETONURIA ( 8 FDA reports)
LEUKOCYTOSIS ( 8 FDA reports)
LIVER DISORDER ( 8 FDA reports)
LUNG DISORDER ( 8 FDA reports)
LUNG INFECTION ( 8 FDA reports)
LUNG INFILTRATION ( 8 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 8 FDA reports)
MENOPAUSE ( 8 FDA reports)
MIDDLE INSOMNIA ( 8 FDA reports)
MULTIPLE INJURIES ( 8 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 8 FDA reports)
NO ADVERSE EVENT ( 8 FDA reports)
ONYCHOMYCOSIS ( 8 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 8 FDA reports)
ORAL INTAKE REDUCED ( 8 FDA reports)
PERIPHERAL COLDNESS ( 8 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 8 FDA reports)
RECTAL POLYP ( 8 FDA reports)
RESPIRATORY DEPRESSION ( 8 FDA reports)
RESPIRATORY TRACT INFECTION ( 8 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 8 FDA reports)
SELF-MEDICATION ( 8 FDA reports)
SENSATION OF HEAVINESS ( 8 FDA reports)
SENSORY LOSS ( 8 FDA reports)
SKIN DISORDER ( 8 FDA reports)
SNEEZING ( 8 FDA reports)
STATUS EPILEPTICUS ( 8 FDA reports)
SUDDEN DEATH ( 8 FDA reports)
SURGERY ( 8 FDA reports)
TENDERNESS ( 8 FDA reports)
TENOSYNOVITIS ( 8 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 8 FDA reports)
THROAT TIGHTNESS ( 8 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 8 FDA reports)
URINARY RETENTION ( 8 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 8 FDA reports)
ABDOMINAL PAIN LOWER ( 7 FDA reports)
AFFECTIVE DISORDER ( 7 FDA reports)
BLOOD BILIRUBIN INCREASED ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 7 FDA reports)
BLOOD POTASSIUM DECREASED ( 7 FDA reports)
BODY TEMPERATURE INCREASED ( 7 FDA reports)
BREECH PRESENTATION ( 7 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 7 FDA reports)
CEREBROVASCULAR DISORDER ( 7 FDA reports)
CHEILITIS ( 7 FDA reports)
CHOLECYSTITIS ACUTE ( 7 FDA reports)
COLONIC POLYP ( 7 FDA reports)
CONGENITAL HYDROCEPHALUS ( 7 FDA reports)
DECREASED INTEREST ( 7 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 7 FDA reports)
DIGEORGE'S SYNDROME ( 7 FDA reports)
EYELID PTOSIS CONGENITAL ( 7 FDA reports)
FIBROMYALGIA ( 7 FDA reports)
FIBULA FRACTURE ( 7 FDA reports)
FLIGHT OF IDEAS ( 7 FDA reports)
GASTROINTESTINAL INJURY ( 7 FDA reports)
GOUT ( 7 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 7 FDA reports)
HEPATIC FAILURE ( 7 FDA reports)
HIP FRACTURE ( 7 FDA reports)
HUNGER ( 7 FDA reports)
HYDRONEPHROSIS ( 7 FDA reports)
HYPERLIPIDAEMIA ( 7 FDA reports)
HYPOKALAEMIA ( 7 FDA reports)
HYPONATRAEMIA ( 7 FDA reports)
ILEAL STENOSIS ( 7 FDA reports)
INCONTINENCE ( 7 FDA reports)
INJECTION SITE REACTION ( 7 FDA reports)
INJURY CORNEAL ( 7 FDA reports)
INTESTINAL OBSTRUCTION ( 7 FDA reports)
IRON DEFICIENCY ANAEMIA ( 7 FDA reports)
LIMB INJURY ( 7 FDA reports)
LIVEDO RETICULARIS ( 7 FDA reports)
LUNG NEOPLASM MALIGNANT ( 7 FDA reports)
METRORRHAGIA ( 7 FDA reports)
MONOCYTE COUNT INCREASED ( 7 FDA reports)
MULTIPLE ALLERGIES ( 7 FDA reports)
MUSCLE RIGIDITY ( 7 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 7 FDA reports)
MYOCARDIAL ISCHAEMIA ( 7 FDA reports)
OBSESSIVE THOUGHTS ( 7 FDA reports)
ORAL PAIN ( 7 FDA reports)
PHARYNGEAL OEDEMA ( 7 FDA reports)
POST PROCEDURAL COMPLICATION ( 7 FDA reports)
PRURITUS ANI ( 7 FDA reports)
PSYCHIATRIC SYMPTOM ( 7 FDA reports)
RASH MACULAR ( 7 FDA reports)
RESPIRATORY RATE INCREASED ( 7 FDA reports)
RIB FRACTURE ( 7 FDA reports)
SINUS HEADACHE ( 7 FDA reports)
SKIN HAEMORRHAGE ( 7 FDA reports)
SLEEP TALKING ( 7 FDA reports)
SLUGGISHNESS ( 7 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 7 FDA reports)
SPLENOMEGALY ( 7 FDA reports)
STRABISMUS ( 7 FDA reports)
TENDON RUPTURE ( 7 FDA reports)
TENSION ( 7 FDA reports)
TOOTHACHE ( 7 FDA reports)
URINE OUTPUT DECREASED ( 7 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 7 FDA reports)
ABORTION INDUCED ( 6 FDA reports)
ANKLE FRACTURE ( 6 FDA reports)
ANORGASMIA ( 6 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 6 FDA reports)
ANXIETY DISORDER ( 6 FDA reports)
APPLICATION SITE ERYTHEMA ( 6 FDA reports)
BACTERIAL DISEASE CARRIER ( 6 FDA reports)
BACTERIAL INFECTION ( 6 FDA reports)
BLOOD CALCIUM DECREASED ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 6 FDA reports)
BODY TEMPERATURE DECREASED ( 6 FDA reports)
BONE DENSITY DECREASED ( 6 FDA reports)
BREAST CANCER IN SITU ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
CHANGE IN SUSTAINED ATTENTION ( 6 FDA reports)
CHONDROMALACIA ( 6 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 6 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 6 FDA reports)
CORONARY ARTERY OCCLUSION ( 6 FDA reports)
CREPITATIONS ( 6 FDA reports)
CYSTITIS ( 6 FDA reports)
DECUBITUS ULCER ( 6 FDA reports)
DIVERTICULUM INTESTINAL ( 6 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 6 FDA reports)
DRUG INTOLERANCE ( 6 FDA reports)
DRUG LEVEL INCREASED ( 6 FDA reports)
DRUG SCREEN NEGATIVE ( 6 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 6 FDA reports)
EMPYEMA ( 6 FDA reports)
ERYTHEMA MULTIFORME ( 6 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 6 FDA reports)
EYE DISCHARGE ( 6 FDA reports)
EYE DISORDER ( 6 FDA reports)
EYE HAEMORRHAGE ( 6 FDA reports)
EYE SWELLING ( 6 FDA reports)
FEELING OF DESPAIR ( 6 FDA reports)
FOOD CRAVING ( 6 FDA reports)
FOOT DEFORMITY ( 6 FDA reports)
FORMICATION ( 6 FDA reports)
GASTROENTERITIS ( 6 FDA reports)
HYDROPNEUMOTHORAX ( 6 FDA reports)
HYPERACUSIS ( 6 FDA reports)
HYPERCHOLESTEROLAEMIA ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
HYPOMANIA ( 6 FDA reports)
IMPRISONMENT ( 6 FDA reports)
INTESTINAL FISTULA ( 6 FDA reports)
JOINT INJURY ( 6 FDA reports)
JUVENILE ARTHRITIS ( 6 FDA reports)
LACERATION ( 6 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 6 FDA reports)
LIP DISCOLOURATION ( 6 FDA reports)
MAMMOPLASTY ( 6 FDA reports)
MASTICATION DISORDER ( 6 FDA reports)
METASTASES TO LYMPH NODES ( 6 FDA reports)
MICTURITION URGENCY ( 6 FDA reports)
OESOPHAGEAL RUPTURE ( 6 FDA reports)
OESOPHAGITIS ( 6 FDA reports)
OSTEORADIONECROSIS ( 6 FDA reports)
OXYGEN SATURATION DECREASED ( 6 FDA reports)
PARAESTHESIA ORAL ( 6 FDA reports)
PERONEAL NERVE PALSY ( 6 FDA reports)
PHARYNGITIS ( 6 FDA reports)
PHOBIA ( 6 FDA reports)
PHOTOPHOBIA ( 6 FDA reports)
POLYSUBSTANCE ABUSE ( 6 FDA reports)
PRODUCT ADHESION ISSUE ( 6 FDA reports)
PROTRUSION TONGUE ( 6 FDA reports)
PRURITUS GENERALISED ( 6 FDA reports)
PULMONARY AIR LEAKAGE ( 6 FDA reports)
PULMONARY FIBROSIS ( 6 FDA reports)
PYELONEPHRITIS ( 6 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 6 FDA reports)
SCRATCH ( 6 FDA reports)
SEXUAL DYSFUNCTION ( 6 FDA reports)
SINGLE UMBILICAL ARTERY ( 6 FDA reports)
SKIN WARM ( 6 FDA reports)
SLEEP APNOEA SYNDROME ( 6 FDA reports)
THERAPY NON-RESPONDER ( 6 FDA reports)
THROAT IRRITATION ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
TIBIA FRACTURE ( 6 FDA reports)
TONGUE OEDEMA ( 6 FDA reports)
TONGUE PARALYSIS ( 6 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 6 FDA reports)
UNDERDOSE ( 6 FDA reports)
VAGINAL HAEMORRHAGE ( 6 FDA reports)
VASCULITIS ( 6 FDA reports)
WRONG DRUG ADMINISTERED ( 6 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 5 FDA reports)
ACUTE PSYCHOSIS ( 5 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
ADENOCARCINOMA ( 5 FDA reports)
ANTEROGRADE AMNESIA ( 5 FDA reports)
APHAGIA ( 5 FDA reports)
APPENDICECTOMY ( 5 FDA reports)
APPLICATION SITE IRRITATION ( 5 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 5 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 5 FDA reports)
BACTERAEMIA ( 5 FDA reports)
BILIARY DYSKINESIA ( 5 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
BONE MARROW DISORDER ( 5 FDA reports)
BREAST CALCIFICATIONS ( 5 FDA reports)
BREAST MASS ( 5 FDA reports)
CARDIAC MURMUR ( 5 FDA reports)
CATATONIA ( 5 FDA reports)
COAGULOPATHY ( 5 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 5 FDA reports)
CONSTRICTED AFFECT ( 5 FDA reports)
DIABETIC NEUROPATHY ( 5 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 5 FDA reports)
DRUG EFFECT INCREASED ( 5 FDA reports)
DRUG PRESCRIBING ERROR ( 5 FDA reports)
EAR DISORDER ( 5 FDA reports)
ENCEPHALOPATHY ( 5 FDA reports)
EPILEPSY ( 5 FDA reports)
EYE MOVEMENT DISORDER ( 5 FDA reports)
FACIAL PAIN ( 5 FDA reports)
FEAR OF DEATH ( 5 FDA reports)
FLANK PAIN ( 5 FDA reports)
FLAT FEET ( 5 FDA reports)
FOETAL GROWTH RETARDATION ( 5 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 5 FDA reports)
GALLBLADDER PAIN ( 5 FDA reports)
GASTRIC HAEMORRHAGE ( 5 FDA reports)
GASTRITIS EROSIVE ( 5 FDA reports)
GASTROINTESTINAL PAIN ( 5 FDA reports)
GINGIVAL BLEEDING ( 5 FDA reports)
GRANULOCYTOPENIA ( 5 FDA reports)
HANGOVER ( 5 FDA reports)
HEPATIC CYST ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
HERPES ZOSTER ( 5 FDA reports)
HIATUS HERNIA ( 5 FDA reports)
HOSPITALISATION ( 5 FDA reports)
HYPOVOLAEMIC SHOCK ( 5 FDA reports)
IMPAIRED SELF-CARE ( 5 FDA reports)
IMPULSE-CONTROL DISORDER ( 5 FDA reports)
INCOHERENT ( 5 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 5 FDA reports)
INJECTION SITE HAEMATOMA ( 5 FDA reports)
INJECTION SITE MASS ( 5 FDA reports)
KIDNEY INFECTION ( 5 FDA reports)
LIP SWELLING ( 5 FDA reports)
LOCAL SWELLING ( 5 FDA reports)
LOSS OF EMPLOYMENT ( 5 FDA reports)
LUPUS-LIKE SYNDROME ( 5 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 5 FDA reports)
MIOSIS ( 5 FDA reports)
MOUTH ULCERATION ( 5 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 5 FDA reports)
MYOCARDITIS ( 5 FDA reports)
NERVE INJURY ( 5 FDA reports)
NONSPECIFIC REACTION ( 5 FDA reports)
OPTIC NEURITIS ( 5 FDA reports)
OSTEOCHONDROSIS ( 5 FDA reports)
OVARIAN CYST ( 5 FDA reports)
PARALYSIS ( 5 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 5 FDA reports)
PHYSICAL ASSAULT ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
PNEUMONIA ASPIRATION ( 5 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 5 FDA reports)
PRODUCT FORMULATION ISSUE ( 5 FDA reports)
PUPILS UNEQUAL ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
RETROGRADE AMNESIA ( 5 FDA reports)
SINUS DISORDER ( 5 FDA reports)
SMALL FOR DATES BABY ( 5 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 5 FDA reports)
SUBSTANCE ABUSE ( 5 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 5 FDA reports)
TONGUE DISCOLOURATION ( 5 FDA reports)
TOOTH LOSS ( 5 FDA reports)
TOXIC SHOCK SYNDROME ( 5 FDA reports)
ULCER HAEMORRHAGE ( 5 FDA reports)
UPPER LIMB FRACTURE ( 5 FDA reports)
UROSEPSIS ( 5 FDA reports)
VENTRICULAR DYSFUNCTION ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
VENTRICULAR HYPERTROPHY ( 5 FDA reports)
VULVAL DISORDER ( 5 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
ACCIDENT ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 4 FDA reports)
ADNEXA UTERI MASS ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
ANAL PRURITUS ( 4 FDA reports)
ANTISOCIAL BEHAVIOUR ( 4 FDA reports)
ANURIA ( 4 FDA reports)
ARTHROPOD BITE ( 4 FDA reports)
ASPIRATION PLEURAL CAVITY ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BILE DUCT OBSTRUCTION ( 4 FDA reports)
BILE DUCT STONE ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 4 FDA reports)
BRAIN NEOPLASM ( 4 FDA reports)
BREAKTHROUGH PAIN ( 4 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 4 FDA reports)
BURSITIS ( 4 FDA reports)
CALCULUS URETERIC ( 4 FDA reports)
CARDIAC FLUTTER ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CHOKING SENSATION ( 4 FDA reports)
CHOLECYSTITIS ( 4 FDA reports)
CHOLECYSTITIS INFECTIVE ( 4 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 4 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
DANDY-WALKER SYNDROME ( 4 FDA reports)
DERMATITIS CONTACT ( 4 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 4 FDA reports)
DIFFICULTY IN WALKING ( 4 FDA reports)
DISINHIBITION ( 4 FDA reports)
DYSPHORIA ( 4 FDA reports)
EATING DISORDER ( 4 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 4 FDA reports)
ELEVATED MOOD ( 4 FDA reports)
ENDOCARDITIS BACTERIAL ( 4 FDA reports)
ENDODONTIC PROCEDURE ( 4 FDA reports)
EUPHORIC MOOD ( 4 FDA reports)
EYE IRRITATION ( 4 FDA reports)
FACIAL BONES FRACTURE ( 4 FDA reports)
FACIAL PALSY ( 4 FDA reports)
FLAT AFFECT ( 4 FDA reports)
FRUSTRATION ( 4 FDA reports)
GALLBLADDER POLYP ( 4 FDA reports)
GENERALISED ANXIETY DISORDER ( 4 FDA reports)
GLOSSODYNIA ( 4 FDA reports)
GRANDIOSITY ( 4 FDA reports)
GUN SHOT WOUND ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HAEMORRHAGIC DIATHESIS ( 4 FDA reports)
HEAD BANGING ( 4 FDA reports)
HEARING IMPAIRED ( 4 FDA reports)
HEMIPARESIS ( 4 FDA reports)
HEPATIC PAIN ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
HYPERPHAGIA ( 4 FDA reports)
HYPERTHYROIDISM ( 4 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 4 FDA reports)
HYPOPHAGIA ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 4 FDA reports)
INCREASED TENDENCY TO BRUISE ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 4 FDA reports)
INTRA-UTERINE DEATH ( 4 FDA reports)
IRREGULAR SLEEP PHASE ( 4 FDA reports)
JAUNDICE ( 4 FDA reports)
JOINT CREPITATION ( 4 FDA reports)
LARYNGOSPASM ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
MASS ( 4 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 4 FDA reports)
MICROCYTIC ANAEMIA ( 4 FDA reports)
MYOPIA ( 4 FDA reports)
NEOPLASM ( 4 FDA reports)
NEOPLASM MALIGNANT ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
OCULAR HYPERAEMIA ( 4 FDA reports)
OLIGOMENORRHOEA ( 4 FDA reports)
OPEN WOUND ( 4 FDA reports)
PETECHIAE ( 4 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 4 FDA reports)
PHOTOSENSITIVITY REACTION ( 4 FDA reports)
PLEURAL FIBROSIS ( 4 FDA reports)
PLEURITIC PAIN ( 4 FDA reports)
PRODUCTIVE COUGH ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
PSORIASIS ( 4 FDA reports)
PULMONARY CONGESTION ( 4 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 4 FDA reports)
PULSE ABSENT ( 4 FDA reports)
RASH PAPULAR ( 4 FDA reports)
RASH PUSTULAR ( 4 FDA reports)
REBOUND EFFECT ( 4 FDA reports)
RECTAL ABSCESS ( 4 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 4 FDA reports)
REGURGITATION ( 4 FDA reports)
RENAL COLIC ( 4 FDA reports)
RENAL CYST ( 4 FDA reports)
ROSACEA ( 4 FDA reports)
SALIVARY HYPERSECRETION ( 4 FDA reports)
SARCOIDOSIS ( 4 FDA reports)
SINUS CONGESTION ( 4 FDA reports)
SJOGREN'S SYNDROME ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
SOCIAL PROBLEM ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
STRESS FRACTURE ( 4 FDA reports)
STUPOR ( 4 FDA reports)
SUBCUTANEOUS ABSCESS ( 4 FDA reports)
TENDON INJURY ( 4 FDA reports)
TESTICULAR PAIN ( 4 FDA reports)
THOUGHT INSERTION ( 4 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 4 FDA reports)
TONGUE DISORDER ( 4 FDA reports)
TONGUE ULCERATION ( 4 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 4 FDA reports)
TRAUMATIC LUNG INJURY ( 4 FDA reports)
URINARY HESITATION ( 4 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 4 FDA reports)
URINE KETONE BODY PRESENT ( 4 FDA reports)
UTERINE LEIOMYOMA ( 4 FDA reports)
VASODILATATION ( 4 FDA reports)
VERBAL ABUSE ( 4 FDA reports)
VIRAL INFECTION ( 4 FDA reports)
VISUAL FIELD DEFECT ( 4 FDA reports)
VITAMIN D DECREASED ( 4 FDA reports)
WHIPLASH INJURY ( 4 FDA reports)
ABNORMAL FAECES ( 3 FDA reports)
ACCIDENTAL DEATH ( 3 FDA reports)
ACCIDENTAL EXPOSURE ( 3 FDA reports)
AGORAPHOBIA ( 3 FDA reports)
AMMONIA INCREASED ( 3 FDA reports)
AMPHETAMINES POSITIVE ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 3 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 3 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 3 FDA reports)
APHONIA ( 3 FDA reports)
APPLICATION SITE PRURITUS ( 3 FDA reports)
ARACHNOID CYST ( 3 FDA reports)
AREFLEXIA ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
ARTHROSCOPIC SURGERY ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
AXILLARY VEIN THROMBOSIS ( 3 FDA reports)
BINGE EATING ( 3 FDA reports)
BLOOD ALCOHOL INCREASED ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BLOOD TEST ABNORMAL ( 3 FDA reports)
BONE LESION ( 3 FDA reports)
BRADYPHRENIA ( 3 FDA reports)
BRAIN INJURY ( 3 FDA reports)
BREAST CYST ( 3 FDA reports)
BREAST DYSPLASIA ( 3 FDA reports)
BREAST ENLARGEMENT ( 3 FDA reports)
BREAST NECROSIS ( 3 FDA reports)
BREAST PAIN ( 3 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
CARDIAC VALVE DISEASE ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CATARACT OPERATION ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 3 FDA reports)
CHANGE OF BOWEL HABIT ( 3 FDA reports)
CHEMOTHERAPY ( 3 FDA reports)
CHEST TUBE INSERTION ( 3 FDA reports)
CHOKING ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 3 FDA reports)
CORONARY ARTERY STENOSIS ( 3 FDA reports)
DEBRIDEMENT ( 3 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DEMYELINATION ( 3 FDA reports)
DEPENDENCE ( 3 FDA reports)
DEPRESSION SUICIDAL ( 3 FDA reports)
DEPRESSIVE SYMPTOM ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DEVICE DISLOCATION ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DIZZINESS EXERTIONAL ( 3 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
DRUG LEVEL DECREASED ( 3 FDA reports)
DRY THROAT ( 3 FDA reports)
DYSLIPIDAEMIA ( 3 FDA reports)
EARLY MORNING AWAKENING ( 3 FDA reports)
ECZEMA NUMMULAR ( 3 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 3 FDA reports)
EMPYEMA DRAINAGE ( 3 FDA reports)
ENDOMETRIAL DISORDER ( 3 FDA reports)
ENURESIS ( 3 FDA reports)
ERYTHEMA NODOSUM ( 3 FDA reports)
ESSENTIAL HYPERTENSION ( 3 FDA reports)
EXOPHTHALMOS ( 3 FDA reports)
EXOSTOSIS ( 3 FDA reports)
EYELID FUNCTION DISORDER ( 3 FDA reports)
EYELID OEDEMA ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FEAR OF DISEASE ( 3 FDA reports)
FEELING DRUNK ( 3 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 3 FDA reports)
FEMALE SEXUAL DYSFUNCTION ( 3 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 3 FDA reports)
FLUID INTAKE REDUCED ( 3 FDA reports)
FOETAL HEART RATE ABNORMAL ( 3 FDA reports)
FRACTURE ( 3 FDA reports)
FRACTURED SACRUM ( 3 FDA reports)
GASTRIC POLYPS ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
GINGIVAL RECESSION ( 3 FDA reports)
GROWTH RETARDATION ( 3 FDA reports)
HEAD DISCOMFORT ( 3 FDA reports)
HEART TRANSPLANT ( 3 FDA reports)
HEAT STROKE ( 3 FDA reports)
HEPATIC CIRRHOSIS ( 3 FDA reports)
HEPATIC LESION ( 3 FDA reports)
HEPATIC MASS ( 3 FDA reports)
HEPATITIS B ( 3 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 3 FDA reports)
HERPES SIMPLEX DNA TEST POSITIVE ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPERREFLEXIA ( 3 FDA reports)
HYPERTONIC BLADDER ( 3 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 3 FDA reports)
ILEUS ( 3 FDA reports)
IMPATIENCE ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 3 FDA reports)
INADEQUATE ANALGESIA ( 3 FDA reports)
INAPPROPRIATE AFFECT ( 3 FDA reports)
INFUSION SITE CELLULITIS ( 3 FDA reports)
INJECTION SITE SWELLING ( 3 FDA reports)
INTRACARDIAC THROMBUS ( 3 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 3 FDA reports)
JOINT SPRAIN ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
KNEE OPERATION ( 3 FDA reports)
LACRIMATION DECREASED ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LUNG OPERATION ( 3 FDA reports)
LYMPHOEDEMA ( 3 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 3 FDA reports)
MACULOPATHY ( 3 FDA reports)
MADAROSIS ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MELANOCYTIC NAEVUS ( 3 FDA reports)
MENSTRUAL DISORDER ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
MIGRAINE WITH AURA ( 3 FDA reports)
MOANING ( 3 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 3 FDA reports)
MONONUCLEOSIS SYNDROME ( 3 FDA reports)
MULTIPLE FRACTURES ( 3 FDA reports)
MUSCLE FLAP OPERATION ( 3 FDA reports)
MUSCLE RUPTURE ( 3 FDA reports)
MUSCULOSKELETAL DISORDER ( 3 FDA reports)
NASAL ODOUR ( 3 FDA reports)
NASAL SEPTUM DEVIATION ( 3 FDA reports)
NEGATIVISM ( 3 FDA reports)
NEOPLASM PROGRESSION ( 3 FDA reports)
NEURALGIA ( 3 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 3 FDA reports)
OESOPHAGEAL PAIN ( 3 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 3 FDA reports)
OSTEOCHONDROMA ( 3 FDA reports)
PAIN OF SKIN ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PANIC REACTION ( 3 FDA reports)
PAPULE ( 3 FDA reports)
PAROSMIA ( 3 FDA reports)
PARTNER STRESS ( 3 FDA reports)
PELVIC VENOUS THROMBOSIS ( 3 FDA reports)
PERICARDITIS ( 3 FDA reports)
PETIT MAL EPILEPSY ( 3 FDA reports)
PITYRIASIS ROSEA ( 3 FDA reports)
PLANTAR FASCIITIS ( 3 FDA reports)
POLYNEUROPATHY ( 3 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 3 FDA reports)
POSTERIOR CAPSULOTOMY ( 3 FDA reports)
POSTICTAL STATE ( 3 FDA reports)
POSTURE ABNORMAL ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
PROCEDURAL PAIN ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
PYODERMA GANGRENOSUM ( 3 FDA reports)
QRS AXIS ABNORMAL ( 3 FDA reports)
RADIOTHERAPY ( 3 FDA reports)
ROTATOR CUFF REPAIR ( 3 FDA reports)
SENSATION OF PRESSURE ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
SHIFT TO THE LEFT ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SHOPLIFTING ( 3 FDA reports)
SINUS ARRHYTHMIA ( 3 FDA reports)
SINUS OPERATION ( 3 FDA reports)
SKIN ATROPHY ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SKIN FISSURES ( 3 FDA reports)
SKIN SWELLING ( 3 FDA reports)
SLEEP WALKING ( 3 FDA reports)
SLOW RESPONSE TO STIMULI ( 3 FDA reports)
SOMATOSENSORY EVOKED POTENTIALS ABNORMAL ( 3 FDA reports)
SOMNAMBULISM ( 3 FDA reports)
SPINAL CORD DISORDER ( 3 FDA reports)
SPINAL LAMINECTOMY ( 3 FDA reports)
SPLENIC LESION ( 3 FDA reports)
SPONDYLOLISTHESIS ( 3 FDA reports)
SPONDYLOLYSIS ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA ( 3 FDA reports)
STREPTOCOCCAL IDENTIFICATION TEST POSITIVE ( 3 FDA reports)
STREPTOCOCCAL INFECTION ( 3 FDA reports)
SUDDEN CARDIAC DEATH ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 3 FDA reports)
SURGICAL PROCEDURE REPEATED ( 3 FDA reports)
TEARFULNESS ( 3 FDA reports)
TEMPERATURE INTOLERANCE ( 3 FDA reports)
TENDON PAIN ( 3 FDA reports)
THEFT ( 3 FDA reports)
THERMAL BURN ( 3 FDA reports)
THORACOTOMY ( 3 FDA reports)
THYROID NEOPLASM ( 3 FDA reports)
TONSILLAR HYPERTROPHY ( 3 FDA reports)
TOOTH ABSCESS ( 3 FDA reports)
TOXIC ENCEPHALOPATHY ( 3 FDA reports)
TRISMUS ( 3 FDA reports)
UMBILICAL CORD ABNORMALITY ( 3 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 3 FDA reports)
VAGINAL CANCER ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 3 FDA reports)
VIITH NERVE PARALYSIS ( 3 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 3 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
VITRECTOMY ( 3 FDA reports)
WEIGHT GAIN POOR ( 3 FDA reports)
ABDOMEN CRUSHING ( 2 FDA reports)
ACCIDENT AT WORK ( 2 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ADENOMA BENIGN ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ANISOCYTOSIS ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 2 FDA reports)
APERT'S SYNDROME ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
APPLICATION SITE EROSION ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
ARTHRITIS ENTEROPATHIC ( 2 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
ASTROCYTOMA ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
AUTISM SPECTRUM DISORDER ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
BACK INJURY ( 2 FDA reports)
BACTERIA URINE IDENTIFIED ( 2 FDA reports)
BASEDOW'S DISEASE ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
BLADDER PAIN ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD CORTISOL INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BLOOD PROLACTIN INCREASED ( 2 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BREAST CANCER METASTATIC ( 2 FDA reports)
BREAST LUMP REMOVAL ( 2 FDA reports)
BREAST SWELLING ( 2 FDA reports)
BREATH ODOUR ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC DISCOMFORT ( 2 FDA reports)
CAROTID ARTERY DISEASE ( 2 FDA reports)
CARTILAGE INJURY ( 2 FDA reports)
CERVICAL CYST ( 2 FDA reports)
CERVICOBRACHIAL SYNDROME ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
CHOANAL ATRESIA ( 2 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 2 FDA reports)
CHOREA ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA STAGE 0 ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 2 FDA reports)
COELIAC DISEASE ( 2 FDA reports)
COGWHEEL RIGIDITY ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 2 FDA reports)
CONGENITAL AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CONTRAST MEDIA REACTION ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CORONARY ARTERY ANEURYSM ( 2 FDA reports)
CORONARY ARTERY PERFORATION ( 2 FDA reports)
COXSACKIE VIRAL INFECTION ( 2 FDA reports)
CRANIOPHARYNGIOMA ( 2 FDA reports)
CRANIOSYNOSTOSIS ( 2 FDA reports)
CSF PROTEIN INCREASED ( 2 FDA reports)
CYSTITIS HAEMORRHAGIC ( 2 FDA reports)
DAYDREAMING ( 2 FDA reports)
DEATH OF RELATIVE ( 2 FDA reports)
DELIVERY ( 2 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 2 FDA reports)
DRUG TOLERANCE INCREASED ( 2 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
EJACULATION DISORDER ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
ERYTHROMELALGIA ( 2 FDA reports)
EXPOSURE TO TOXIC AGENT ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FAECES HARD ( 2 FDA reports)
FALLOPIAN TUBE CANCER ( 2 FDA reports)
FAMILY STRESS ( 2 FDA reports)
FAT TISSUE INCREASED ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FISTULA ( 2 FDA reports)
FLASHBACK ( 2 FDA reports)
GALACTORRHOEA ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GAMBLING ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRIC PERFORATION ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GENERALISED NON-CONVULSIVE EPILEPSY ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GENITAL HERPES ( 2 FDA reports)
GINGIVAL DISORDER ( 2 FDA reports)
GINGIVAL HYPERPLASIA ( 2 FDA reports)
GLYCOSURIA ( 2 FDA reports)
GRAFT DELAMINATION ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAIR PLUCKING ( 2 FDA reports)
HALLUCINATION, OLFACTORY ( 2 FDA reports)
HAND DEFORMITY ( 2 FDA reports)
HEAD DEFORMITY ( 2 FDA reports)
HEART RATE ABNORMAL ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEPATIC ENZYME DECREASED ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HOMICIDE ( 2 FDA reports)
HYDROURETER ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERMETABOLISM ( 2 FDA reports)
HYPERMETROPIA ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
HYPOTRICHOSIS ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
HYSTERECTOMY ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INCORRECT STORAGE OF DRUG ( 2 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 2 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 2 FDA reports)
INJECTION SITE ATROPHY ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 2 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 2 FDA reports)
INTUSSUSCEPTION ( 2 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 2 FDA reports)
IUD MIGRATION ( 2 FDA reports)
JAW DISORDER ( 2 FDA reports)
JAW FRACTURE ( 2 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LEARNING DISORDER ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LENTIGO ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIVE BIRTH ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LOCHIA MALODOUROUS ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
LYMPHADENECTOMY ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MACROGNATHIA ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MALE SEXUAL DYSFUNCTION ( 2 FDA reports)
MASTITIS ( 2 FDA reports)
MASTOIDITIS ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 2 FDA reports)
MITRAL VALVE PROLAPSE ( 2 FDA reports)
MUCOUS STOOLS ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NASAL DISCOMFORT ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NASAL SEPTUM ULCERATION ( 2 FDA reports)
NECK INJURY ( 2 FDA reports)
NEOPLASM RECURRENCE ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NOCARDIOSIS ( 2 FDA reports)
NODULE ON EXTREMITY ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OLIGODIPSIA ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
OTITIS EXTERNA ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
OVARIAN DISORDER ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 2 FDA reports)
PAPILLOMA VIRAL INFECTION ( 2 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 2 FDA reports)
PARENT-CHILD PROBLEM ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PITUITARY TUMOUR BENIGN ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
POLYHYDRAMNIOS ( 2 FDA reports)
POLYMENORRHOEA ( 2 FDA reports)
POLYP ( 2 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 2 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PRODUCT LABEL ISSUE ( 2 FDA reports)
PRODUCT PHYSICAL ISSUE ( 2 FDA reports)
PRODUCT TAMPERING ( 2 FDA reports)
PROMOTION OF PERIPHERAL CIRCULATION ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PSYCHOTIC BEHAVIOUR ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PULMONARY THROMBOSIS ( 2 FDA reports)
PULSE PRESSURE INCREASED ( 2 FDA reports)
PURPURA ( 2 FDA reports)
READING DISORDER ( 2 FDA reports)
RECTAL PROLAPSE ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 2 FDA reports)
RENIN INCREASED ( 2 FDA reports)
RESIDUAL URINE ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
SCAB ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SCHOOL REFUSAL ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SCROTAL OEDEMA ( 2 FDA reports)
SCROTAL PAIN ( 2 FDA reports)
SEASONAL ALLERGY ( 2 FDA reports)
SELF-INJURIOUS IDEATION ( 2 FDA reports)
SEROMA ( 2 FDA reports)
SEXUAL ABUSE ( 2 FDA reports)
SEXUAL ASSAULT VICTIM ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SKIN ODOUR ABNORMAL ( 2 FDA reports)
SPINAL CORD NEOPLASM ( 2 FDA reports)
STARVATION ( 2 FDA reports)
SYNDACTYLY ( 2 FDA reports)
TACHYPHRENIA ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TESTICULAR RETRACTION ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
THROAT LESION ( 2 FDA reports)
THYROID CYST ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TOBACCO USER ( 2 FDA reports)
TONIC CLONIC MOVEMENTS ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TOOTH RESORPTION ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TOURETTE'S DISORDER ( 2 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 2 FDA reports)
TUBERCULIN TEST POSITIVE ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
UTERINE INFECTION ( 2 FDA reports)
UTERINE POLYP ( 2 FDA reports)
VAGINAL INFECTION ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
WEGENER'S GRANULOMATOSIS ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
ALLERGY TO PLANTS ( 1 FDA reports)
ALOPECIA AREATA ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANO-RECTAL STENOSIS ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 1 FDA reports)
AORTIC SURGERY ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
APPLICATION SITE HAEMATOMA ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE PAPULES ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
APPLICATION SITE URTICARIA ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARTERIAL INJURY ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPERGER'S DISORDER ( 1 FDA reports)
ATROPHY OF GLOBE ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF EYELID ( 1 FDA reports)
BILATERAL BREAST BUDS ( 1 FDA reports)
BILIARY ADENOMA ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CANNABINOIDS INCREASED ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BONE ABSCESS ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BORDERLINE GLAUCOMA ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BUCCOGLOSSAL SYNDROME ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BURKITT'S LYMPHOMA ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 1 FDA reports)
CEPHALHAEMATOMA ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL FUNGAL INFECTION ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL HYGROMA ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CHLOROPSIA ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLONUS ( 1 FDA reports)
COAGULATION FACTOR IX LEVEL DECREASED ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 1 FDA reports)
CONJUNCTIVITIS VIRAL ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CRYSTAL URINE PRESENT ( 1 FDA reports)
CSF IMMUNOGLOBULIN INCREASED ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CYST ASPIRATION ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DACRYOSTENOSIS CONGENITAL ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DELAYED PUBERTY ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS INFECTED ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DISSOCIATIVE FUGUE ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DIURETIC ABUSE ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRESSLER'S SYNDROME ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSHIDROSIS ( 1 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
ECZEMA INFECTED ( 1 FDA reports)
EJACULATION DELAYED ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCONVULSIVE THERAPY ( 1 FDA reports)
ENDOCARDIAL FIBROELASTOSIS ( 1 FDA reports)
ENDOMETRIAL CANCER METASTATIC ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
ERYTHROPSIA ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXCESSIVE MASTURBATION ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXERCISE CAPACITY DECREASED ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXHIBITIONISM ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACTOR VIII INHIBITION ( 1 FDA reports)
FAECAL VOLUME DECREASED ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FIGHT IN SCHOOL ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GAIT SPASTIC ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GALLBLADDER NECROSIS ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GASTROSCHISIS ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL INFECTION FEMALE ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GINGIVECTOMY ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HEAD TITUBATION ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HODGKIN'S DISEASE STAGE II ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPNAGOGIC HALLUCINATION ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOMENORRHOEA ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INGROWN HAIR ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE DISCHARGE ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE INSERTION ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
JAMAIS VU ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JEJUNAL ULCER ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACTATION DISORDER ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LARYNGEAL MASS ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LATENT TUBERCULOSIS ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEARNING DISABILITY ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
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LIP DISORDER ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE III ( 1 FDA reports)
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LUNG NEOPLASM ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
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MACULAR OEDEMA ( 1 FDA reports)
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MATERNAL USE OF ILLICIT DRUGS ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDICAL DEVICE REMOVAL ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGOCELE ( 1 FDA reports)
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MICROCYTOSIS ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 1 FDA reports)
MOLE EXCISION ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
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MUSCLE STRAIN ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOCARDITIS BACTERIAL ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
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MYOPERICARDITIS ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NEAR DROWNING ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEEDLE ISSUE ( 1 FDA reports)
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NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
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NICOTINE DEPENDENCE ( 1 FDA reports)
NIPPLE OEDEMA ( 1 FDA reports)
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NOCTIPHOBIA ( 1 FDA reports)
NODAL OSTEOARTHRITIS ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
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NOSOCOMIAL INFECTION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OCULOGYRIC CRISIS ( 1 FDA reports)
OESOPHAGEAL OEDEMA ( 1 FDA reports)
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ONYCHOLYSIS ( 1 FDA reports)
ONYCHOPHAGIA ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
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ORAL BACTERIAL INFECTION ( 1 FDA reports)
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ORTHOPNOEA ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OVARIAN CYST RUPTURED ( 1 FDA reports)
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OVERWEIGHT ( 1 FDA reports)
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PANCREATIC INSUFFICIENCY ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
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PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARAESTHESIA CIRCUMORAL ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PARATHYROID TUMOUR BENIGN ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
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PATHOGEN RESISTANCE ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
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POST CONCUSSION SYNDROME ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
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RECTAL DISCHARGE ( 1 FDA reports)
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RED BLOOD CELLS URINE ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
REGRESSIVE BEHAVIOUR ( 1 FDA reports)
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