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

AMNESIA ( 337 FDA reports)
SOMNAMBULISM ( 228 FDA reports)
DRUG INEFFECTIVE ( 215 FDA reports)
NAUSEA ( 198 FDA reports)
ROAD TRAFFIC ACCIDENT ( 189 FDA reports)
FALL ( 188 FDA reports)
PAIN ( 181 FDA reports)
FATIGUE ( 150 FDA reports)
ANXIETY ( 134 FDA reports)
HEADACHE ( 125 FDA reports)
DYSPNOEA ( 124 FDA reports)
IMPAIRED DRIVING ABILITY ( 119 FDA reports)
INSOMNIA ( 113 FDA reports)
DEPRESSION ( 112 FDA reports)
VOMITING ( 111 FDA reports)
DIZZINESS ( 110 FDA reports)
ARTHRALGIA ( 94 FDA reports)
LOSS OF CONSCIOUSNESS ( 93 FDA reports)
DIARRHOEA ( 89 FDA reports)
CHEST PAIN ( 87 FDA reports)
BACK PAIN ( 86 FDA reports)
SOMNOLENCE ( 86 FDA reports)
CONFUSIONAL STATE ( 84 FDA reports)
CONTUSION ( 83 FDA reports)
ABNORMAL BEHAVIOUR ( 78 FDA reports)
ASTHENIA ( 74 FDA reports)
WEIGHT INCREASED ( 72 FDA reports)
GAIT DISTURBANCE ( 69 FDA reports)
PAIN IN EXTREMITY ( 69 FDA reports)
SUICIDAL IDEATION ( 69 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 69 FDA reports)
WEIGHT DECREASED ( 68 FDA reports)
FEELING ABNORMAL ( 64 FDA reports)
HALLUCINATION ( 60 FDA reports)
ABDOMINAL PAIN ( 55 FDA reports)
CONDITION AGGRAVATED ( 54 FDA reports)
HYPERTENSION ( 53 FDA reports)
INJURY ( 53 FDA reports)
PULMONARY EMBOLISM ( 52 FDA reports)
ABDOMINAL PAIN UPPER ( 50 FDA reports)
PYREXIA ( 50 FDA reports)
TREMOR ( 50 FDA reports)
HYPOAESTHESIA ( 49 FDA reports)
URINARY TRACT INFECTION ( 49 FDA reports)
MALAISE ( 48 FDA reports)
SYNCOPE ( 48 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 47 FDA reports)
AGGRESSION ( 46 FDA reports)
AGITATION ( 46 FDA reports)
PNEUMONIA ( 46 FDA reports)
HYPOTENSION ( 45 FDA reports)
CONVULSION ( 43 FDA reports)
HYPERHIDROSIS ( 43 FDA reports)
PALPITATIONS ( 43 FDA reports)
DIABETES MELLITUS ( 42 FDA reports)
DRUG INTERACTION ( 42 FDA reports)
OEDEMA PERIPHERAL ( 42 FDA reports)
RASH ( 42 FDA reports)
DEHYDRATION ( 41 FDA reports)
DRUG ABUSE ( 41 FDA reports)
INCORRECT DOSE ADMINISTERED ( 41 FDA reports)
CONSTIPATION ( 40 FDA reports)
HEAD INJURY ( 40 FDA reports)
CONCUSSION ( 39 FDA reports)
DRUG DEPENDENCE ( 39 FDA reports)
NECK PAIN ( 38 FDA reports)
OVERDOSE ( 38 FDA reports)
PRURITUS ( 37 FDA reports)
DEATH ( 35 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 35 FDA reports)
MUSCULOSKELETAL PAIN ( 35 FDA reports)
MYALGIA ( 35 FDA reports)
PARAESTHESIA ( 35 FDA reports)
PRODUCT QUALITY ISSUE ( 35 FDA reports)
EMOTIONAL DISTRESS ( 34 FDA reports)
OFF LABEL USE ( 34 FDA reports)
SLEEP WALKING ( 34 FDA reports)
STRESS ( 34 FDA reports)
NIGHTMARE ( 33 FDA reports)
DEEP VEIN THROMBOSIS ( 32 FDA reports)
TYPE 2 DIABETES MELLITUS ( 32 FDA reports)
ANAEMIA ( 31 FDA reports)
MEMORY IMPAIRMENT ( 31 FDA reports)
PANIC ATTACK ( 31 FDA reports)
BALANCE DISORDER ( 30 FDA reports)
CEREBROVASCULAR ACCIDENT ( 30 FDA reports)
CHILLS ( 30 FDA reports)
COUGH ( 30 FDA reports)
DYSARTHRIA ( 30 FDA reports)
OSTEOARTHRITIS ( 30 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 29 FDA reports)
SLEEP-RELATED EATING DISORDER ( 29 FDA reports)
BLOOD GLUCOSE INCREASED ( 28 FDA reports)
CHEST DISCOMFORT ( 28 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 28 FDA reports)
RESPIRATORY FAILURE ( 28 FDA reports)
VISION BLURRED ( 28 FDA reports)
ABDOMINAL DISCOMFORT ( 27 FDA reports)
DECREASED APPETITE ( 27 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 27 FDA reports)
SLEEP TALKING ( 27 FDA reports)
DISORIENTATION ( 26 FDA reports)
MUSCLE SPASMS ( 26 FDA reports)
SINUSITIS ( 26 FDA reports)
ATRIAL FIBRILLATION ( 25 FDA reports)
BRADYCARDIA ( 25 FDA reports)
DYSPHAGIA ( 25 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 25 FDA reports)
SKIN LACERATION ( 25 FDA reports)
SUICIDE ATTEMPT ( 25 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 24 FDA reports)
IRRITABILITY ( 24 FDA reports)
MENTAL DISORDER ( 24 FDA reports)
MIGRAINE ( 24 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 24 FDA reports)
DYSPEPSIA ( 23 FDA reports)
FLUSHING ( 23 FDA reports)
GALLBLADDER DISORDER ( 23 FDA reports)
GASTRITIS ( 23 FDA reports)
INTENTIONAL DRUG MISUSE ( 23 FDA reports)
RIB FRACTURE ( 23 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 23 FDA reports)
DYSKINESIA ( 22 FDA reports)
HEART RATE INCREASED ( 22 FDA reports)
ABDOMINAL DISTENSION ( 21 FDA reports)
CHOLELITHIASIS ( 21 FDA reports)
DRY MOUTH ( 21 FDA reports)
HAEMATOMA ( 21 FDA reports)
JOINT SWELLING ( 21 FDA reports)
MYOCARDIAL INFARCTION ( 21 FDA reports)
ARTHRITIS ( 20 FDA reports)
BURNING SENSATION ( 20 FDA reports)
CHOLECYSTITIS CHRONIC ( 20 FDA reports)
HOT FLUSH ( 20 FDA reports)
MUSCULAR WEAKNESS ( 20 FDA reports)
NERVOUSNESS ( 20 FDA reports)
PSYCHOTIC DISORDER ( 20 FDA reports)
SPEECH DISORDER ( 20 FDA reports)
ABASIA ( 19 FDA reports)
ALOPECIA ( 19 FDA reports)
BLOOD PRESSURE INCREASED ( 19 FDA reports)
DIPLOPIA ( 19 FDA reports)
DRUG DOSE OMISSION ( 19 FDA reports)
DRUG EFFECT DECREASED ( 19 FDA reports)
PANCREATITIS ( 19 FDA reports)
THINKING ABNORMAL ( 19 FDA reports)
URINARY RETENTION ( 19 FDA reports)
BLOOD GLUCOSE DECREASED ( 18 FDA reports)
BLOOD PRESSURE DECREASED ( 18 FDA reports)
COMPLETED SUICIDE ( 18 FDA reports)
EATING DISORDER ( 18 FDA reports)
ERYTHEMA ( 18 FDA reports)
FEELING HOT ( 18 FDA reports)
HALLUCINATION, VISUAL ( 18 FDA reports)
INFLUENZA LIKE ILLNESS ( 18 FDA reports)
INTENTIONAL OVERDOSE ( 18 FDA reports)
NEUROPATHY PERIPHERAL ( 18 FDA reports)
PNEUMONIA ASPIRATION ( 18 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 17 FDA reports)
CARDIAC DISORDER ( 17 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 17 FDA reports)
DELIRIUM ( 17 FDA reports)
HEART RATE IRREGULAR ( 17 FDA reports)
NASOPHARYNGITIS ( 17 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 16 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 16 FDA reports)
DISTURBANCE IN ATTENTION ( 16 FDA reports)
DRY EYE ( 16 FDA reports)
HAEMORRHAGE ( 16 FDA reports)
HEART RATE DECREASED ( 16 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 16 FDA reports)
LACERATION ( 16 FDA reports)
PLATELET COUNT DECREASED ( 16 FDA reports)
POST-TRAUMATIC AMNESTIC DISORDER ( 16 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 16 FDA reports)
PRODUCT ADHESION ISSUE ( 16 FDA reports)
RENAL FAILURE ACUTE ( 16 FDA reports)
RESPIRATORY ARREST ( 16 FDA reports)
SLEEP DISORDER ( 16 FDA reports)
STAPHYLOCOCCAL INFECTION ( 16 FDA reports)
TREATMENT NONCOMPLIANCE ( 16 FDA reports)
VERTIGO ( 16 FDA reports)
WITHDRAWAL SYNDROME ( 16 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 15 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 15 FDA reports)
DYSGEUSIA ( 15 FDA reports)
FLATULENCE ( 15 FDA reports)
HAEMOGLOBIN DECREASED ( 15 FDA reports)
HYPERSENSITIVITY ( 15 FDA reports)
HYPOKALAEMIA ( 15 FDA reports)
MENTAL STATUS CHANGES ( 15 FDA reports)
MIDDLE INSOMNIA ( 15 FDA reports)
OSTEOMYELITIS ( 15 FDA reports)
PAIN IN JAW ( 15 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 15 FDA reports)
RASH PRURITIC ( 15 FDA reports)
SKIN HAEMORRHAGE ( 15 FDA reports)
SLEEP APNOEA SYNDROME ( 15 FDA reports)
TOOTH ABSCESS ( 15 FDA reports)
UPPER LIMB FRACTURE ( 15 FDA reports)
ALCOHOL USE ( 14 FDA reports)
COLON ADENOMA ( 14 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 14 FDA reports)
HAEMORRHOIDS ( 14 FDA reports)
HYPOXIA ( 14 FDA reports)
INJECTION SITE PAIN ( 14 FDA reports)
MOOD SWINGS ( 14 FDA reports)
MOVEMENT DISORDER ( 14 FDA reports)
NEURALGIA ( 14 FDA reports)
NEUTROPENIA ( 14 FDA reports)
OROPHARYNGEAL PAIN ( 14 FDA reports)
PERSONALITY CHANGE ( 14 FDA reports)
PULMONARY HYPERTENSION ( 14 FDA reports)
SPINAL FRACTURE ( 14 FDA reports)
TACHYCARDIA ( 14 FDA reports)
WRIST FRACTURE ( 14 FDA reports)
BONE PAIN ( 13 FDA reports)
BRONCHITIS ( 13 FDA reports)
DELUSION ( 13 FDA reports)
DRUG HYPERSENSITIVITY ( 13 FDA reports)
FEAR ( 13 FDA reports)
GLAUCOMA ( 13 FDA reports)
HEMIPARESIS ( 13 FDA reports)
HYPERLIPIDAEMIA ( 13 FDA reports)
ILL-DEFINED DISORDER ( 13 FDA reports)
INFECTION ( 13 FDA reports)
INITIAL INSOMNIA ( 13 FDA reports)
JOINT INJURY ( 13 FDA reports)
MUSCLE TWITCHING ( 13 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 13 FDA reports)
PARAESTHESIA ORAL ( 13 FDA reports)
PARANOIA ( 13 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 13 FDA reports)
BLOOD POTASSIUM DECREASED ( 12 FDA reports)
BREAKTHROUGH PAIN ( 12 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 12 FDA reports)
CATARACT ( 12 FDA reports)
CHOLECYSTITIS ( 12 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 12 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 12 FDA reports)
EMOTIONAL DISORDER ( 12 FDA reports)
EXCORIATION ( 12 FDA reports)
FEMUR FRACTURE ( 12 FDA reports)
INFLUENZA ( 12 FDA reports)
LIMB INJURY ( 12 FDA reports)
METASTASES TO LIVER ( 12 FDA reports)
OEDEMA ( 12 FDA reports)
POLLAKIURIA ( 12 FDA reports)
PRESYNCOPE ( 12 FDA reports)
RENAL FAILURE ( 12 FDA reports)
RESPIRATORY DEPRESSION ( 12 FDA reports)
SINUS CONGESTION ( 12 FDA reports)
SPINAL OSTEOARTHRITIS ( 12 FDA reports)
SWELLING ( 12 FDA reports)
VISUAL IMPAIRMENT ( 12 FDA reports)
ABNORMAL DREAMS ( 11 FDA reports)
APHASIA ( 11 FDA reports)
BLADDER DISORDER ( 11 FDA reports)
BRADYPHRENIA ( 11 FDA reports)
CARDIAC MURMUR ( 11 FDA reports)
CHOKING ( 11 FDA reports)
CORONARY ARTERY OCCLUSION ( 11 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 11 FDA reports)
DRY SKIN ( 11 FDA reports)
FEELING DRUNK ( 11 FDA reports)
FEELING JITTERY ( 11 FDA reports)
GASTROENTERITIS ( 11 FDA reports)
HIP FRACTURE ( 11 FDA reports)
IMPRISONMENT ( 11 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 11 FDA reports)
METASTASES TO BONE ( 11 FDA reports)
NEPHROLITHIASIS ( 11 FDA reports)
NEUROGENIC BLADDER ( 11 FDA reports)
NIGHT SWEATS ( 11 FDA reports)
OPEN WOUND ( 11 FDA reports)
OSTEONECROSIS OF JAW ( 11 FDA reports)
POOR QUALITY SLEEP ( 11 FDA reports)
PUPIL FIXED ( 11 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 11 FDA reports)
RESTLESSNESS ( 11 FDA reports)
TOOTH DISORDER ( 11 FDA reports)
UNRESPONSIVE TO STIMULI ( 11 FDA reports)
WHEEZING ( 11 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 11 FDA reports)
ANGER ( 10 FDA reports)
ANOREXIA ( 10 FDA reports)
ANXIETY DISORDER ( 10 FDA reports)
APPLICATION SITE RASH ( 10 FDA reports)
ASTHMA ( 10 FDA reports)
ATELECTASIS ( 10 FDA reports)
CARDIAC ARREST ( 10 FDA reports)
CEREBRAL INFARCTION ( 10 FDA reports)
CRYING ( 10 FDA reports)
DENTAL CARIES ( 10 FDA reports)
DIVERTICULUM INTESTINAL ( 10 FDA reports)
ERECTILE DYSFUNCTION ( 10 FDA reports)
EYE PAIN ( 10 FDA reports)
FACIAL PAIN ( 10 FDA reports)
GUN SHOT WOUND ( 10 FDA reports)
IMPAIRED HEALING ( 10 FDA reports)
INADEQUATE ANALGESIA ( 10 FDA reports)
IRRITABLE BOWEL SYNDROME ( 10 FDA reports)
NEOPLASM PROGRESSION ( 10 FDA reports)
NOCTURIA ( 10 FDA reports)
OSTEOPOROSIS ( 10 FDA reports)
PAIN OF SKIN ( 10 FDA reports)
PANCREATIC CARCINOMA ( 10 FDA reports)
PHOTOSENSITIVITY REACTION ( 10 FDA reports)
PLEURAL EFFUSION ( 10 FDA reports)
PRURITUS GENERALISED ( 10 FDA reports)
SEPSIS ( 10 FDA reports)
SWELLING FACE ( 10 FDA reports)
SWOLLEN TONGUE ( 10 FDA reports)
TESTICULAR CYST ( 10 FDA reports)
ABDOMINAL PAIN LOWER ( 9 FDA reports)
BARRETT'S OESOPHAGUS ( 9 FDA reports)
BASAL CELL CARCINOMA ( 9 FDA reports)
BLOOD CREATININE INCREASED ( 9 FDA reports)
CELLULITIS ( 9 FDA reports)
COLON CANCER STAGE III ( 9 FDA reports)
COORDINATION ABNORMAL ( 9 FDA reports)
ECONOMIC PROBLEM ( 9 FDA reports)
EPISTAXIS ( 9 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 9 FDA reports)
FOLLICULITIS ( 9 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 9 FDA reports)
HAEMATOCHEZIA ( 9 FDA reports)
HANGOVER ( 9 FDA reports)
HYDROCELE ( 9 FDA reports)
HYPERAESTHESIA ( 9 FDA reports)
HYPERSOMNIA ( 9 FDA reports)
HYPOPHAGIA ( 9 FDA reports)
INTERSTITIAL LUNG DISEASE ( 9 FDA reports)
JOINT SPRAIN ( 9 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 9 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 9 FDA reports)
LETHARGY ( 9 FDA reports)
LIVER INJURY ( 9 FDA reports)
NERVOUS SYSTEM DISORDER ( 9 FDA reports)
OSTEONECROSIS ( 9 FDA reports)
PARAPLEGIA ( 9 FDA reports)
RADIUS FRACTURE ( 9 FDA reports)
RESTLESS LEGS SYNDROME ( 9 FDA reports)
SKIN SWELLING ( 9 FDA reports)
SKIN WARM ( 9 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 9 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 9 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 9 FDA reports)
WOUND INFECTION FUNGAL ( 9 FDA reports)
ADVERSE EVENT ( 8 FDA reports)
ANHEDONIA ( 8 FDA reports)
APPLICATION SITE ERYTHEMA ( 8 FDA reports)
BLOOD ALBUMIN DECREASED ( 8 FDA reports)
BLOOD SODIUM DECREASED ( 8 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 8 FDA reports)
CARDIO-RESPIRATORY ARREST ( 8 FDA reports)
CARDIOMEGALY ( 8 FDA reports)
COGNITIVE DISORDER ( 8 FDA reports)
COLONIC POLYP ( 8 FDA reports)
DEPRESSED MOOD ( 8 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 8 FDA reports)
DROOLING ( 8 FDA reports)
DRUG ADMINISTRATION ERROR ( 8 FDA reports)
DRUG TOLERANCE ( 8 FDA reports)
FIBROMYALGIA ( 8 FDA reports)
GLOBULINS INCREASED ( 8 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 8 FDA reports)
HAEMATOCRIT DECREASED ( 8 FDA reports)
HALLUCINATION, AUDITORY ( 8 FDA reports)
HEPATIC ENZYME INCREASED ( 8 FDA reports)
HYPONATRAEMIA ( 8 FDA reports)
IMPAIRED WORK ABILITY ( 8 FDA reports)
LEGAL PROBLEM ( 8 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 8 FDA reports)
MOBILITY DECREASED ( 8 FDA reports)
MULTIPLE MYELOMA ( 8 FDA reports)
MULTIPLE SCLEROSIS ( 8 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 8 FDA reports)
PERONEAL NERVE PALSY ( 8 FDA reports)
PNEUMOTHORAX ( 8 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 8 FDA reports)
PROSTATE CANCER ( 8 FDA reports)
RHEUMATOID ARTHRITIS ( 8 FDA reports)
ROTATOR CUFF SYNDROME ( 8 FDA reports)
SEDATION ( 8 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 8 FDA reports)
SINUS TACHYCARDIA ( 8 FDA reports)
SKIN CANCER ( 8 FDA reports)
SKIN ULCER ( 8 FDA reports)
SPINAL COLUMN STENOSIS ( 8 FDA reports)
SPINAL DISORDER ( 8 FDA reports)
SYNCOPE VASOVAGAL ( 8 FDA reports)
TARDIVE DYSKINESIA ( 8 FDA reports)
TESTICULAR PAIN ( 8 FDA reports)
URTICARIA ( 8 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 8 FDA reports)
ACCIDENTAL OVERDOSE ( 7 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 7 FDA reports)
APNOEA ( 7 FDA reports)
ARTHROPATHY ( 7 FDA reports)
BACK DISORDER ( 7 FDA reports)
BURSITIS ( 7 FDA reports)
CATATONIA ( 7 FDA reports)
DISEASE PROGRESSION ( 7 FDA reports)
DYSPHONIA ( 7 FDA reports)
DYSSTASIA ( 7 FDA reports)
EXOSTOSIS ( 7 FDA reports)
FEELING COLD ( 7 FDA reports)
GASTRIC HAEMORRHAGE ( 7 FDA reports)
GASTRIC ULCER ( 7 FDA reports)
GLOSSODYNIA ( 7 FDA reports)
HAEMATURIA ( 7 FDA reports)
HAND FRACTURE ( 7 FDA reports)
HYPERGLYCAEMIA ( 7 FDA reports)
HYPOTHERMIA ( 7 FDA reports)
ILEITIS ( 7 FDA reports)
INCOHERENT ( 7 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 7 FDA reports)
JAW FRACTURE ( 7 FDA reports)
LEUKOPENIA ( 7 FDA reports)
LUNG DISORDER ( 7 FDA reports)
MOOD ALTERED ( 7 FDA reports)
MOUTH ULCERATION ( 7 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 7 FDA reports)
NEOPLASM MALIGNANT ( 7 FDA reports)
PHARYNGEAL OEDEMA ( 7 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 7 FDA reports)
PROTEIN TOTAL INCREASED ( 7 FDA reports)
PSORIASIS ( 7 FDA reports)
PULMONARY FIBROSIS ( 7 FDA reports)
RASH ERYTHEMATOUS ( 7 FDA reports)
RENAL FAILURE CHRONIC ( 7 FDA reports)
RHABDOMYOLYSIS ( 7 FDA reports)
SCAR ( 7 FDA reports)
SCREAMING ( 7 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 7 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 7 FDA reports)
THROMBOSIS ( 7 FDA reports)
TRAUMATIC BRAIN INJURY ( 7 FDA reports)
URINARY INCONTINENCE ( 7 FDA reports)
VENTRICULAR TACHYCARDIA ( 7 FDA reports)
ABDOMINAL TENDERNESS ( 6 FDA reports)
ANOXIC ENCEPHALOPATHY ( 6 FDA reports)
BILIARY DYSKINESIA ( 6 FDA reports)
BIPOLAR DISORDER ( 6 FDA reports)
BLADDER DYSFUNCTION ( 6 FDA reports)
BLISTER ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 6 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 6 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
BRAIN CONTUSION ( 6 FDA reports)
CANDIDIASIS ( 6 FDA reports)
CAUDA EQUINA SYNDROME ( 6 FDA reports)
DEFORMITY ( 6 FDA reports)
DERMATITIS CONTACT ( 6 FDA reports)
DROWNING ( 6 FDA reports)
DUODENITIS ( 6 FDA reports)
DYSURIA ( 6 FDA reports)
EAR PAIN ( 6 FDA reports)
ERUCTATION ( 6 FDA reports)
EYE SWELLING ( 6 FDA reports)
FACE INJURY ( 6 FDA reports)
FACET JOINT SYNDROME ( 6 FDA reports)
FLANK PAIN ( 6 FDA reports)
FUNGAL INFECTION ( 6 FDA reports)
GASTRIC DISORDER ( 6 FDA reports)
GASTROINTESTINAL DISORDER ( 6 FDA reports)
GASTROINTESTINAL TOXICITY ( 6 FDA reports)
GINGIVAL PAIN ( 6 FDA reports)
GRAND MAL CONVULSION ( 6 FDA reports)
HYPERKALAEMIA ( 6 FDA reports)
HYPOTHYROIDISM ( 6 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 6 FDA reports)
INTENTIONAL SELF-INJURY ( 6 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 6 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 6 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 6 FDA reports)
JAW DISORDER ( 6 FDA reports)
LIP SWELLING ( 6 FDA reports)
LOCALISED INFECTION ( 6 FDA reports)
MANIA ( 6 FDA reports)
MEDICATION ERROR ( 6 FDA reports)
MULTIPLE DRUG OVERDOSE ( 6 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 6 FDA reports)
MUSCLE STRAIN ( 6 FDA reports)
NO THERAPEUTIC RESPONSE ( 6 FDA reports)
ORAL PAIN ( 6 FDA reports)
OXYGEN SATURATION DECREASED ( 6 FDA reports)
PHYSICAL ASSAULT ( 6 FDA reports)
POST CONCUSSION SYNDROME ( 6 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 6 FDA reports)
PULMONARY OEDEMA ( 6 FDA reports)
RASH MACULAR ( 6 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
SKULL FRACTURED BASE ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
TOOTH FRACTURE ( 6 FDA reports)
TOOTH INFECTION ( 6 FDA reports)
TRANCE ( 6 FDA reports)
UNEVALUABLE EVENT ( 6 FDA reports)
URINARY TRACT DISORDER ( 6 FDA reports)
VAGINAL DISCHARGE ( 6 FDA reports)
ACCIDENT ( 5 FDA reports)
ACIDOSIS ( 5 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 5 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 5 FDA reports)
ATAXIA ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 5 FDA reports)
BLOOD CALCIUM DECREASED ( 5 FDA reports)
BRAIN COMPRESSION ( 5 FDA reports)
BREAST CANCER ( 5 FDA reports)
BREAST MASS ( 5 FDA reports)
CHONDROPATHY ( 5 FDA reports)
COELIAC DISEASE ( 5 FDA reports)
CROHN'S DISEASE ( 5 FDA reports)
DEVICE MALFUNCTION ( 5 FDA reports)
DIABETIC NEUROPATHY ( 5 FDA reports)
DRUG PRESCRIBING ERROR ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
EAR INFECTION ( 5 FDA reports)
EMPHYSEMA ( 5 FDA reports)
EYE DISORDER ( 5 FDA reports)
FACIAL BONES FRACTURE ( 5 FDA reports)
HEARING IMPAIRED ( 5 FDA reports)
HEPATIC STEATOSIS ( 5 FDA reports)
HYPERPHAGIA ( 5 FDA reports)
HYPERTONIA ( 5 FDA reports)
HYPOKINESIA ( 5 FDA reports)
INJECTION SITE ERYTHEMA ( 5 FDA reports)
INJECTION SITE HAEMATOMA ( 5 FDA reports)
JOINT DISLOCATION ( 5 FDA reports)
JOINT STIFFNESS ( 5 FDA reports)
KNEE DEFORMITY ( 5 FDA reports)
LIGAMENT RUPTURE ( 5 FDA reports)
LOWER LIMB FRACTURE ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
MAJOR DEPRESSION ( 5 FDA reports)
MASKED FACIES ( 5 FDA reports)
METASTASES TO LYMPH NODES ( 5 FDA reports)
MIOSIS ( 5 FDA reports)
MITRAL VALVE CALCIFICATION ( 5 FDA reports)
MITRAL VALVE DISEASE ( 5 FDA reports)
MITRAL VALVE INCOMPETENCE ( 5 FDA reports)
MULTIPLE FRACTURES ( 5 FDA reports)
MULTIPLE INJURIES ( 5 FDA reports)
OBESITY ( 5 FDA reports)
ORAL INFECTION ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
PANIC DISORDER ( 5 FDA reports)
PARALYSIS ( 5 FDA reports)
PARKINSON'S DISEASE ( 5 FDA reports)
PELVIC FRACTURE ( 5 FDA reports)
PERICARDIAL EFFUSION ( 5 FDA reports)
PERIORBITAL HAEMATOMA ( 5 FDA reports)
POISONING ( 5 FDA reports)
PROCEDURAL PAIN ( 5 FDA reports)
RADICULOPATHY ( 5 FDA reports)
RAYNAUD'S PHENOMENON ( 5 FDA reports)
RHINORRHOEA ( 5 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 5 FDA reports)
SCIATICA ( 5 FDA reports)
SENSORY LOSS ( 5 FDA reports)
SINUS DISORDER ( 5 FDA reports)
SPINAL COMPRESSION FRACTURE ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 5 FDA reports)
SUBDURAL HAEMATOMA ( 5 FDA reports)
THYROID DISORDER ( 5 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 5 FDA reports)
TONGUE DISORDER ( 5 FDA reports)
TOOTHACHE ( 5 FDA reports)
TRAUMATIC LUNG INJURY ( 5 FDA reports)
TYPE 1 DIABETES MELLITUS ( 5 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
VIRAL INFECTION ( 5 FDA reports)
VISUAL MIDLINE SHIFT SYNDROME ( 5 FDA reports)
ABORTION SPONTANEOUS ( 4 FDA reports)
ACCIDENT AT WORK ( 4 FDA reports)
ACCIDENTAL EXPOSURE ( 4 FDA reports)
ACUTE RESPIRATORY FAILURE ( 4 FDA reports)
ADRENAL HAEMORRHAGE ( 4 FDA reports)
ADVERSE DRUG REACTION ( 4 FDA reports)
AGEUSIA ( 4 FDA reports)
AMENORRHOEA ( 4 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
AORTIC CALCIFICATION ( 4 FDA reports)
APPLICATION SITE REACTION ( 4 FDA reports)
ATRIAL SEPTAL DEFECT ( 4 FDA reports)
BILIARY COLIC ( 4 FDA reports)
BLEEDING TIME PROLONGED ( 4 FDA reports)
BLOOD PRESSURE ABNORMAL ( 4 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 4 FDA reports)
BREAST CANCER METASTATIC ( 4 FDA reports)
BREAST CANCER RECURRENT ( 4 FDA reports)
CARPAL TUNNEL SYNDROME ( 4 FDA reports)
CATARACT OPERATION ( 4 FDA reports)
CEREBROSCLEROSIS ( 4 FDA reports)
CHAPPED LIPS ( 4 FDA reports)
COLON CANCER RECURRENT ( 4 FDA reports)
CRANIAL NERVE DISORDER ( 4 FDA reports)
CYSTITIS ( 4 FDA reports)
DEVICE FAILURE ( 4 FDA reports)
DIABETIC COMA ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
DRUG SCREEN POSITIVE ( 4 FDA reports)
DUODENAL ULCER ( 4 FDA reports)
DYSPAREUNIA ( 4 FDA reports)
ENCEPHALITIS HERPES ( 4 FDA reports)
ENDODONTIC PROCEDURE ( 4 FDA reports)
ENURESIS ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
EXPOSED BONE IN JAW ( 4 FDA reports)
EYE IRRITATION ( 4 FDA reports)
EYELID PTOSIS ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
FIBROMA ( 4 FDA reports)
GASTROENTERITIS VIRAL ( 4 FDA reports)
GENERALISED ANXIETY DISORDER ( 4 FDA reports)
GINGIVAL BLEEDING ( 4 FDA reports)
GROIN PAIN ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HALLUCINATIONS, MIXED ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
HIATUS HERNIA ( 4 FDA reports)
HORMONE LEVEL ABNORMAL ( 4 FDA reports)
HUMERUS FRACTURE ( 4 FDA reports)
HYPERTHYROIDISM ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
HYPOVITAMINOSIS ( 4 FDA reports)
HYSTERECTOMY ( 4 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
INJECTION SITE DISCOLOURATION ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
KIDNEY INFECTION ( 4 FDA reports)
KYPHOSIS ( 4 FDA reports)
LARGE INTESTINE PERFORATION ( 4 FDA reports)
LIBIDO INCREASED ( 4 FDA reports)
LIMB CRUSHING INJURY ( 4 FDA reports)
LOOSE TOOTH ( 4 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE II ( 4 FDA reports)
LUNG INJURY ( 4 FDA reports)
MACROCYTOSIS ( 4 FDA reports)
MENIERE'S DISEASE ( 4 FDA reports)
MENISCUS LESION ( 4 FDA reports)
METASTASES TO SPINE ( 4 FDA reports)
METASTATIC NEOPLASM ( 4 FDA reports)
MIXED HYPERLIPIDAEMIA ( 4 FDA reports)
MUSCLE ATROPHY ( 4 FDA reports)
MUSCLE INJURY ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
OBSTRUCTION GASTRIC ( 4 FDA reports)
OEDEMA MOUTH ( 4 FDA reports)
OESOPHAGITIS ( 4 FDA reports)
OSTEOLYSIS ( 4 FDA reports)
OSTEOMYELITIS FUNGAL ( 4 FDA reports)
PANCREATIC CYST ( 4 FDA reports)
PARONYCHIA ( 4 FDA reports)
PATHOLOGICAL FRACTURE ( 4 FDA reports)
PATHOLOGICAL GAMBLING ( 4 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 4 FDA reports)
PHOTOPHOBIA ( 4 FDA reports)
POST PROCEDURAL INFECTION ( 4 FDA reports)
PROSTATIC CALCIFICATION ( 4 FDA reports)
PSYCHIATRIC SYMPTOM ( 4 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
RASH PAPULAR ( 4 FDA reports)
RENAL PAIN ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
RETCHING ( 4 FDA reports)
SEASONAL ALLERGY ( 4 FDA reports)
SEBORRHOEIC KERATOSIS ( 4 FDA reports)
SEXUAL ABUSE ( 4 FDA reports)
SEXUAL DYSFUNCTION ( 4 FDA reports)
SHOCK HAEMORRHAGIC ( 4 FDA reports)
SINUS BRADYCARDIA ( 4 FDA reports)
SLEEP SEX ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
STILLBIRTH ( 4 FDA reports)
SURGERY ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 4 FDA reports)
TENDERNESS ( 4 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 4 FDA reports)
THERAPEUTIC RESPONSE PROLONGED ( 4 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 4 FDA reports)
TINNITUS ( 4 FDA reports)
TROPONIN INCREASED ( 4 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
VASCULAR CALCIFICATION ( 4 FDA reports)
VASCULITIS ( 4 FDA reports)
VENOUS INSUFFICIENCY ( 4 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 4 FDA reports)
VULVAL DISORDER ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ADNEXA UTERI PAIN ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
ANKLE FRACTURE ( 3 FDA reports)
APPLICATION SITE BURN ( 3 FDA reports)
APPLICATION SITE PRURITUS ( 3 FDA reports)
APPLICATION SITE SCAR ( 3 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 3 FDA reports)
B-CELL LYMPHOMA ( 3 FDA reports)
BACK INJURY ( 3 FDA reports)
BILE DUCT OBSTRUCTION ( 3 FDA reports)
BLEPHAROSPASM ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 3 FDA reports)
BLOOD MAGNESIUM DECREASED ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BLOOD URINE PRESENT ( 3 FDA reports)
BREAST PAIN ( 3 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CEREBELLAR ATROPHY ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
CHRONIC SINUSITIS ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
CLAVICLE FRACTURE ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
COLITIS ( 3 FDA reports)
COLITIS ULCERATIVE ( 3 FDA reports)
COMA ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
COSTOCHONDRITIS ( 3 FDA reports)
DEAFNESS UNILATERAL ( 3 FDA reports)
DECUBITUS ULCER ( 3 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DEVICE LEAKAGE ( 3 FDA reports)
DIASTOLIC DYSFUNCTION ( 3 FDA reports)
DILATATION ATRIAL ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
DREAMY STATE ( 3 FDA reports)
DRUG ABUSER ( 3 FDA reports)
DRUG EFFECT INCREASED ( 3 FDA reports)
DRUG TOLERANCE INCREASED ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
DYSTONIA ( 3 FDA reports)
EAR DISCOMFORT ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 3 FDA reports)
ENERGY INCREASED ( 3 FDA reports)
EXPIRED DRUG ADMINISTERED ( 3 FDA reports)
FACIAL PARESIS ( 3 FDA reports)
FAECAL INCONTINENCE ( 3 FDA reports)
FAILURE TO THRIVE ( 3 FDA reports)
FAMILY STRESS ( 3 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 3 FDA reports)
FOOD CRAVING ( 3 FDA reports)
FUNGAL SKIN INFECTION ( 3 FDA reports)
FURUNCLE ( 3 FDA reports)
GALACTORRHOEA ( 3 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 3 FDA reports)
GINGIVAL SWELLING ( 3 FDA reports)
GLOBAL AMNESIA ( 3 FDA reports)
GLOSSITIS ( 3 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
HELICOBACTER INFECTION ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HERNIA ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
HYDROCEPHALUS ( 3 FDA reports)
HYPERACUSIS ( 3 FDA reports)
HYPERPARATHYROIDISM ( 3 FDA reports)
HYPOAESTHESIA FACIAL ( 3 FDA reports)
HYPOPNOEA ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
ILEUS ( 3 FDA reports)
INCISION SITE INFECTION ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
INJECTION SITE EXTRAVASATION ( 3 FDA reports)
INJECTION SITE HAEMORRHAGE ( 3 FDA reports)
INJECTION SITE PRURITUS ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
INJECTION SITE SWELLING ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
IUD MIGRATION ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
KETOACIDOSIS ( 3 FDA reports)
LACRIMATION INCREASED ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LISTLESS ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
LUMBAR SPINAL STENOSIS ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
MARITAL PROBLEM ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MENOPAUSE ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
METRORRHAGIA ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX IMMUNE RESTORATION DISEASE ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
NECK INJURY ( 3 FDA reports)
NEPHROPATHY ( 3 FDA reports)
NERVE COMPRESSION ( 3 FDA reports)
NERVE INJURY ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
NODULE ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 3 FDA reports)
OCULAR HYPERAEMIA ( 3 FDA reports)
ORAL DISCOMFORT ( 3 FDA reports)
OVARIAN CYST ( 3 FDA reports)
PANCREATITIS CHRONIC ( 3 FDA reports)
PAROSMIA ( 3 FDA reports)
PELVIC PAIN ( 3 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 3 FDA reports)
POST PROCEDURAL DISCOMFORT ( 3 FDA reports)
POST PROCEDURAL HAEMATOMA ( 3 FDA reports)
PRECANCEROUS CELLS PRESENT ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PULMONARY HAEMORRHAGE ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
READING DISORDER ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RECTAL ULCER ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
SALIVARY HYPERSECRETION ( 3 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SINUS HEADACHE ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SKIN IRRITATION ( 3 FDA reports)
SKIN LESION ( 3 FDA reports)
SKIN ODOUR ABNORMAL ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
SYNOVIAL CYST ( 3 FDA reports)
TENSION HEADACHE ( 3 FDA reports)
THERMAL BURN ( 3 FDA reports)
TONGUE BITING ( 3 FDA reports)
TOOTH LOSS ( 3 FDA reports)
TRIGGER FINGER ( 3 FDA reports)
VAGINAL HAEMORRHAGE ( 3 FDA reports)
VASCULAR INJURY ( 3 FDA reports)
VENOUS INJURY ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
VITAMIN B12 DEFICIENCY ( 3 FDA reports)
VITAMIN D DEFICIENCY ( 3 FDA reports)
WEIGHT BEARING DIFFICULTY ( 3 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ACCIDENTAL DEATH ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ADRENAL MASS ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ALCOHOL POISONING ( 2 FDA reports)
ALLERGY TO METALS ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
APPLICATION SITE EXCORIATION ( 2 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 2 FDA reports)
APPLICATION SITE PERSPIRATION ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ARTERY DISSECTION ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ATRIAL HYPERTROPHY ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BELLIGERENCE ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLADDER NEOPLASM ( 2 FDA reports)
BLADDER OPERATION ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BLOOD VISCOSITY INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE DENSITY DECREASED ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CARDIAC PACEMAKER INSERTION ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CARTILAGE INJURY ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHEST INJURY ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHOREA ( 2 FDA reports)
COAGULATION TIME PROLONGED ( 2 FDA reports)
COCCIDIOIDOMYCOSIS ( 2 FDA reports)
COLLAPSE OF LUNG ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
CORNEAL ABRASION ( 2 FDA reports)
CORNEAL OPACITY ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYSTOCELE ( 2 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DEPRESSIVE SYMPTOM ( 2 FDA reports)
DEVICE BREAKAGE ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISSOCIATION ( 2 FDA reports)
DROP ATTACKS ( 2 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 2 FDA reports)
DRUG EFFECT PROLONGED ( 2 FDA reports)
DRUG INTERACTION POTENTIATION ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ENDOMETRIOSIS ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
ESSENTIAL HYPERTENSION ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GINGIVAL RECESSION ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEAD TITUBATION ( 2 FDA reports)
HEART DISEASE CONGENITAL ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HOMICIDE ( 2 FDA reports)
HOSTILITY ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPERTRICHOSIS ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE CELLULITIS ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INJECTION SITE PAPULE ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTESTINAL RESECTION ( 2 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 2 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LACTASE DEFICIENCY ( 2 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LHERMITTE'S SIGN ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIP DRY ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LIVER TRANSPLANT ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LOSS OF BLADDER SENSATION ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
MITRAL VALVE PROLAPSE ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NASAL MUCOSAL DISORDER ( 2 FDA reports)
NEUROGENIC BOWEL ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
NODAL RHYTHM ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OESOPHAGEAL DISORDER ( 2 FDA reports)
OESOPHAGEAL PAIN ( 2 FDA reports)
ONYCHOMYCOSIS ( 2 FDA reports)
OPPORTUNISTIC INFECTION ( 2 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
OVARIAN MASS ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PATELLA FRACTURE ( 2 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHYSICAL ABUSE ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PRECANCEROUS MUCOSAL LESION ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROSTATIC OBSTRUCTION ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PSYCHOLOGICAL TRAUMA ( 2 FDA reports)
PULMONARY ARTERY ATRESIA ( 2 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
QUALITY OF LIFE DECREASED ( 2 FDA reports)
RADICULITIS ( 2 FDA reports)
REBOUND EFFECT ( 2 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
RENAL INJURY ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
RIGHT ATRIAL DILATATION ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SELF ESTEEM DECREASED ( 2 FDA reports)
SELF-INJURIOUS IDEATION ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SHOPLIFTING ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SKIN MASS ( 2 FDA reports)
SKULL FRACTURE ( 2 FDA reports)
SMALL INTESTINAL PERFORATION ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SPINAL FUSION SURGERY ( 2 FDA reports)
SPLENIC RUPTURE ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STEATORRHOEA ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUICIDAL BEHAVIOUR ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
TEMPORAL ARTERITIS ( 2 FDA reports)
TENSION ( 2 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
THERAPY REGIMEN CHANGED ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
THYROXINE INCREASED ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 2 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 2 FDA reports)
TRICUSPID VALVE DISEASE ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
UMBILICAL HERNIA ( 2 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 2 FDA reports)
URETHRAL CARUNCLE ( 2 FDA reports)
URETHRAL POLYP ( 2 FDA reports)
URINARY HESITATION ( 2 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 2 FDA reports)
URINE ODOUR ABNORMAL ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VASCULAR INSUFFICIENCY ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VEIN PAIN ( 2 FDA reports)
VENOUS OCCLUSION ( 2 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 2 FDA reports)
VITAMIN B12 DECREASED ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
VOCAL CORD DISORDER ( 2 FDA reports)
VULVOVAGINAL PRURITUS ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
WHIPLASH INJURY ( 2 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ABORTED PREGNANCY ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTEROGRADE AMNESIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPLICATION SITE DRYNESS ( 1 FDA reports)
APPLICATION SITE INFECTION ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
APPLICATION SITE ULCER ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
APPLICATION SITE WARMTH ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AUTOMATISM ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIAL TEST ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BENIGN OESOPHAGEAL NEOPLASM ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER PROLAPSE ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLEPHAROPLASTY ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE ATROPHY ( 1 FDA reports)
BONE CANCER METASTATIC ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE FRAGMENTATION ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE NEOPLASM MALIGNANT ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRACHIAL PLEXOPATHY ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BURN OF INTERNAL ORGANS ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATARACT NUCLEAR ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COMMINUTED FRACTURE ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
COUGH DECREASED ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYST ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DECOMPRESSION SICKNESS ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DENTAL NECROSIS ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELDERLY ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOSCOPY SMALL INTESTINE ABNORMAL ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
FACE AND MOUTH X-RAY ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FAECAL DISIMPACTION ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FROSTBITE ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GINGIVAL ERYTHEMA ( 1 FDA reports)
GINGIVAL INFECTION ( 1 FDA reports)
GINGIVAL PRURITUS ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
GUTTATE PSORIASIS ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HORDEOLUM ( 1 FDA reports)
HUMAN EHRLICHIOSIS ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPNOPOMPIC HALLUCINATION ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
IMPULSE-CONTROL DISORDER ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE ABSCESS STERILE ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
IUCD COMPLICATION ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABORATORY TEST ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LEGIONELLA TEST ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUPUS ENCEPHALITIS ( 1 FDA reports)
LUPUS ENTERITIS ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOTOR NEURONE DISEASE ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEUROCYSTICERCOSIS ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NODULE ON EXTREMITY ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OBSTRUCTIVE CHRONIC BRONCHITIS WITH ACUTE EXACERBATION ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
ONYCHALGIA ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
OPEN FRACTURE ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL CAVITY FISTULA ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORCHITIS ( 1 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERIDIVERTICULAR ABSCESS ( 1 FDA reports)
PERIODONTAL INFECTION ( 1 FDA reports)
PERIODONTAL OPERATION ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PITUITARY TUMOUR RECURRENT ( 1 FDA reports)
PLATELET AGGREGATION INCREASED ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMOBILIA ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYP ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
PORPHYRIA ACUTE ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PRESCRIPTION FORM TAMPERING ( 1 FDA reports)
PRODUCT COMMINGLING ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 1 FDA reports)
PROGESTERONE INCREASED ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROSTATIC PAIN ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY PNEUMATOCELE ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULMONARY VALVE DISEASE ( 1 FDA reports)
PULPITIS DENTAL ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RADICULITIS LUMBOSACRAL ( 1 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
REHABILITATION THERAPY ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL OSTEODYSTROPHY ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETINITIS PIGMENTOSA ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
SCHIRMER'S TEST ABNORMAL ( 1 FDA reports)
SCLERAL DISCOLOURATION ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SEPTIC RASH ( 1 FDA reports)
SHARED PSYCHOTIC DISORDER ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL CORD INJURY THORACIC ( 1 FDA reports)
SPINAL ROD INSERTION ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SPOUSAL ABUSE ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 1 FDA reports)
STARING ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STICKY SKIN ( 1 FDA reports)
STREPTOCOCCAL ABSCESS ( 1 FDA reports)
STUBBORNNESS ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUPERINFECTION BACTERIAL ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 1 FDA reports)
TATTOO ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
TETANY ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THIRST ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THYROGLOSSAL CYST ( 1 FDA reports)
THYROID MASS ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
TIC ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOOTH SOCKET HAEMORRHAGE ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UPPER EXTREMITY MASS ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URETHRAL SPASM ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINE BILIRUBIN INCREASED ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
UTERINE PAIN ( 1 FDA reports)
UTERINE RUPTURE ( 1 FDA reports)
UTERINE SPASM ( 1 FDA reports)
VAGINAL SWELLING ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VICTIM OF SEXUAL ABUSE ( 1 FDA reports)
VIOLENT IDEATION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITELLO-INTESTINAL DUCT REMNANT ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
VULVAR DYSPLASIA ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WRIST DEFORMITY ( 1 FDA reports)
YAWNING ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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