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

PAIN ( 942 FDA reports)
ANXIETY ( 823 FDA reports)
INJURY ( 817 FDA reports)
RENAL FAILURE ( 740 FDA reports)
UNEVALUABLE EVENT ( 683 FDA reports)
FEAR ( 615 FDA reports)
EMOTIONAL DISTRESS ( 611 FDA reports)
RENAL INJURY ( 529 FDA reports)
ANHEDONIA ( 494 FDA reports)
STRESS ( 437 FDA reports)
RENAL IMPAIRMENT ( 436 FDA reports)
MULTI-ORGAN FAILURE ( 347 FDA reports)
DEPRESSION ( 340 FDA reports)
DEATH ( 336 FDA reports)
CEREBROVASCULAR ACCIDENT ( 176 FDA reports)
RENAL FAILURE ACUTE ( 163 FDA reports)
NAUSEA ( 147 FDA reports)
DYSPNOEA ( 134 FDA reports)
ANAEMIA ( 129 FDA reports)
OSTEONECROSIS OF JAW ( 128 FDA reports)
FALL ( 116 FDA reports)
VOMITING ( 115 FDA reports)
PAIN IN EXTREMITY ( 113 FDA reports)
OSTEOARTHRITIS ( 111 FDA reports)
DIARRHOEA ( 105 FDA reports)
MYOCARDIAL INFARCTION ( 105 FDA reports)
PYREXIA ( 105 FDA reports)
ABDOMINAL PAIN ( 103 FDA reports)
HYPERTENSION ( 102 FDA reports)
INSOMNIA ( 102 FDA reports)
BACK PAIN ( 97 FDA reports)
HYPOTENSION ( 96 FDA reports)
PAIN IN JAW ( 96 FDA reports)
CONSTIPATION ( 95 FDA reports)
OSTEOMYELITIS ( 93 FDA reports)
DEEP VEIN THROMBOSIS ( 89 FDA reports)
PNEUMONIA ( 89 FDA reports)
ARTHRALGIA ( 88 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 88 FDA reports)
METASTASES TO BONE ( 87 FDA reports)
OEDEMA PERIPHERAL ( 86 FDA reports)
HEADACHE ( 85 FDA reports)
DISABILITY ( 80 FDA reports)
MUSCULOSKELETAL PAIN ( 79 FDA reports)
WEIGHT DECREASED ( 79 FDA reports)
CARDIOMEGALY ( 77 FDA reports)
NERVOUSNESS ( 77 FDA reports)
PLEURAL EFFUSION ( 77 FDA reports)
BONE DISORDER ( 75 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 74 FDA reports)
FATIGUE ( 73 FDA reports)
RESPIRATORY FAILURE ( 72 FDA reports)
DIZZINESS ( 71 FDA reports)
DYSPHAGIA ( 71 FDA reports)
SWELLING ( 71 FDA reports)
RASH ( 70 FDA reports)
CHEST PAIN ( 68 FDA reports)
CELLULITIS ( 67 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 67 FDA reports)
TOOTHACHE ( 66 FDA reports)
ATRIAL FIBRILLATION ( 65 FDA reports)
CARDIAC DISORDER ( 61 FDA reports)
IMPAIRED HEALING ( 61 FDA reports)
SPINAL OSTEOARTHRITIS ( 61 FDA reports)
ARTHRITIS ( 60 FDA reports)
CONFUSIONAL STATE ( 60 FDA reports)
VISION BLURRED ( 60 FDA reports)
URINARY TRACT INFECTION ( 59 FDA reports)
OSTEITIS ( 58 FDA reports)
OSTEOPOROSIS ( 56 FDA reports)
BRONCHITIS ( 54 FDA reports)
DECREASED APPETITE ( 54 FDA reports)
ERYTHEMA ( 54 FDA reports)
NEUROPATHY PERIPHERAL ( 54 FDA reports)
ASTHENIA ( 53 FDA reports)
BONE PAIN ( 53 FDA reports)
LOOSE TOOTH ( 52 FDA reports)
MITRAL VALVE INCOMPETENCE ( 52 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 50 FDA reports)
INFECTION ( 50 FDA reports)
SYNCOPE ( 50 FDA reports)
COUGH ( 49 FDA reports)
DEFORMITY ( 49 FDA reports)
HAEMORRHOIDS ( 49 FDA reports)
HYPOAESTHESIA ( 48 FDA reports)
GINGIVAL PAIN ( 46 FDA reports)
ARTHROPATHY ( 45 FDA reports)
BONE LESION ( 45 FDA reports)
LUNG NEOPLASM ( 44 FDA reports)
OEDEMA ( 44 FDA reports)
SLEEP APNOEA SYNDROME ( 44 FDA reports)
HIP FRACTURE ( 43 FDA reports)
HYPOPHAGIA ( 43 FDA reports)
MASTICATION DISORDER ( 43 FDA reports)
ORGAN FAILURE ( 43 FDA reports)
RENAL FAILURE CHRONIC ( 43 FDA reports)
SEPSIS ( 43 FDA reports)
TREMOR ( 43 FDA reports)
HAEMATOCHEZIA ( 42 FDA reports)
HYPOKALAEMIA ( 42 FDA reports)
OSTEONECROSIS ( 42 FDA reports)
PRURITUS ( 42 FDA reports)
ARTERIOSCLEROSIS ( 41 FDA reports)
CHONDROLYSIS ( 41 FDA reports)
DENTAL CARIES ( 41 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 41 FDA reports)
HIATUS HERNIA ( 41 FDA reports)
PNEUMOTHORAX ( 41 FDA reports)
URTICARIA ( 41 FDA reports)
AFFECTIVE DISORDER ( 40 FDA reports)
GASTRITIS ( 40 FDA reports)
STAPHYLOCOCCAL INFECTION ( 40 FDA reports)
THROMBOCYTOPENIA ( 40 FDA reports)
ATELECTASIS ( 39 FDA reports)
CARDIAC MURMUR ( 39 FDA reports)
COMPRESSION FRACTURE ( 39 FDA reports)
FEAR OF DEATH ( 39 FDA reports)
NECK PAIN ( 39 FDA reports)
GAIT DISTURBANCE ( 38 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 38 FDA reports)
SCAR ( 38 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 37 FDA reports)
DYSPEPSIA ( 37 FDA reports)
LUNG INFILTRATION ( 37 FDA reports)
METASTASES TO SPINE ( 37 FDA reports)
TOOTH EXTRACTION ( 37 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 37 FDA reports)
CHOLELITHIASIS ( 36 FDA reports)
ASTHMA ( 35 FDA reports)
EXOSTOSIS ( 35 FDA reports)
HYPERLIPIDAEMIA ( 35 FDA reports)
MALAISE ( 35 FDA reports)
RECTAL HAEMORRHAGE ( 35 FDA reports)
EPISTAXIS ( 34 FDA reports)
FACET JOINT SYNDROME ( 34 FDA reports)
SINUSITIS ( 34 FDA reports)
CONVULSION ( 33 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 33 FDA reports)
PULMONARY FIBROSIS ( 33 FDA reports)
TOOTH ABSCESS ( 33 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 33 FDA reports)
EXPOSED BONE IN JAW ( 32 FDA reports)
JOINT EFFUSION ( 32 FDA reports)
NIGHT SWEATS ( 32 FDA reports)
PHARYNGITIS ( 32 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 31 FDA reports)
CARDIAC ARREST ( 31 FDA reports)
DECREASED INTEREST ( 31 FDA reports)
GINGIVAL INFECTION ( 31 FDA reports)
BREAST CANCER RECURRENT ( 30 FDA reports)
CARDIO-RESPIRATORY ARREST ( 30 FDA reports)
LOCALISED INFECTION ( 30 FDA reports)
SKIN DISORDER ( 30 FDA reports)
SYNOVIAL CYST ( 30 FDA reports)
BLOOD PRESSURE INCREASED ( 29 FDA reports)
HEAD INJURY ( 29 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 29 FDA reports)
PARAESTHESIA ( 29 FDA reports)
THROMBOSIS ( 29 FDA reports)
BLOOD PRESSURE DECREASED ( 28 FDA reports)
CORONARY ARTERY DISEASE ( 28 FDA reports)
DIVERTICULUM ( 28 FDA reports)
DRY MOUTH ( 28 FDA reports)
FOOT FRACTURE ( 28 FDA reports)
GROIN PAIN ( 28 FDA reports)
PULMONARY EMBOLISM ( 28 FDA reports)
CHILLS ( 27 FDA reports)
CONTUSION ( 27 FDA reports)
DEVICE RELATED INFECTION ( 27 FDA reports)
FLUID OVERLOAD ( 27 FDA reports)
MENTAL DISORDER ( 27 FDA reports)
MUSCLE SPASMS ( 27 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 27 FDA reports)
SCOLIOSIS ( 27 FDA reports)
URINARY RETENTION ( 27 FDA reports)
ADVERSE EVENT ( 26 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 26 FDA reports)
HAEMORRHAGE ( 26 FDA reports)
HYPONATRAEMIA ( 26 FDA reports)
INCONTINENCE ( 26 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 26 FDA reports)
LYMPHADENOPATHY ( 26 FDA reports)
LYMPHOEDEMA ( 26 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 26 FDA reports)
RESPIRATORY DISTRESS ( 26 FDA reports)
SWELLING FACE ( 26 FDA reports)
TENDONITIS ( 26 FDA reports)
CARDIAC FAILURE ( 25 FDA reports)
DYSPNOEA EXERTIONAL ( 25 FDA reports)
HAEMATOMA ( 25 FDA reports)
LUMBAR SPINAL STENOSIS ( 25 FDA reports)
METASTASES TO LUNG ( 25 FDA reports)
OVARIAN CYST ( 25 FDA reports)
TACHYCARDIA ( 25 FDA reports)
AGRANULOCYTOSIS ( 24 FDA reports)
CARDIOGENIC SHOCK ( 24 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 24 FDA reports)
INFLUENZA ( 24 FDA reports)
MENORRHAGIA ( 24 FDA reports)
MENTAL STATUS CHANGES ( 24 FDA reports)
OSTEOPENIA ( 24 FDA reports)
PATHOLOGICAL FRACTURE ( 24 FDA reports)
PSYCHIATRIC SYMPTOM ( 24 FDA reports)
SEPTIC SHOCK ( 24 FDA reports)
SURGERY ( 24 FDA reports)
THROMBOSIS IN DEVICE ( 24 FDA reports)
UNRESPONSIVE TO STIMULI ( 24 FDA reports)
VISUAL IMPAIRMENT ( 24 FDA reports)
BRADYCARDIA ( 23 FDA reports)
BREAST CANCER METASTATIC ( 23 FDA reports)
BURSITIS ( 23 FDA reports)
CARPAL TUNNEL SYNDROME ( 23 FDA reports)
FACIAL BONES FRACTURE ( 23 FDA reports)
HYPERCOAGULATION ( 23 FDA reports)
JOINT SWELLING ( 23 FDA reports)
NEURITIS ( 23 FDA reports)
TENDERNESS ( 23 FDA reports)
BONE DEBRIDEMENT ( 22 FDA reports)
BONE LOSS ( 22 FDA reports)
BONE SCAN ABNORMAL ( 22 FDA reports)
CYSTITIS ( 22 FDA reports)
GINGIVAL OEDEMA ( 22 FDA reports)
HOT FLUSH ( 22 FDA reports)
MUSCULAR WEAKNESS ( 22 FDA reports)
ODYNOPHAGIA ( 22 FDA reports)
ORAL PAIN ( 22 FDA reports)
OSTEOSCLEROSIS ( 22 FDA reports)
PERICARDIAL EFFUSION ( 22 FDA reports)
POLLAKIURIA ( 22 FDA reports)
PULMONARY OEDEMA ( 22 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 22 FDA reports)
BLOOD CREATININE INCREASED ( 21 FDA reports)
FOOT DEFORMITY ( 21 FDA reports)
GINGIVAL SWELLING ( 21 FDA reports)
HALLUCINATION ( 21 FDA reports)
HEPATIC STEATOSIS ( 21 FDA reports)
ILEUS PARALYTIC ( 21 FDA reports)
LETHARGY ( 21 FDA reports)
OXYGEN SATURATION DECREASED ( 21 FDA reports)
PERICARDITIS ( 21 FDA reports)
SINUS TACHYCARDIA ( 21 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 21 FDA reports)
TINNITUS ( 21 FDA reports)
VENTRICULAR HYPERTROPHY ( 21 FDA reports)
APPENDICITIS ( 20 FDA reports)
ARRHYTHMIA ( 20 FDA reports)
CHRONIC SINUSITIS ( 20 FDA reports)
DIABETES MELLITUS ( 20 FDA reports)
EMOTIONAL DISORDER ( 20 FDA reports)
FUNGAL INFECTION ( 20 FDA reports)
HYPERSENSITIVITY ( 20 FDA reports)
JOINT INJURY ( 20 FDA reports)
NEOPLASM MALIGNANT ( 20 FDA reports)
ORAL INFECTION ( 20 FDA reports)
PANCYTOPENIA ( 20 FDA reports)
POST PROCEDURAL COMPLICATION ( 20 FDA reports)
ABDOMINAL DISTENSION ( 19 FDA reports)
ABDOMINAL PAIN UPPER ( 19 FDA reports)
ASCITES ( 19 FDA reports)
BLOOD POTASSIUM DECREASED ( 19 FDA reports)
CHONDROMALACIA ( 19 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 19 FDA reports)
DEPRESSED MOOD ( 19 FDA reports)
DEPRESSIVE SYMPTOM ( 19 FDA reports)
DEVICE FAILURE ( 19 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 19 FDA reports)
GINGIVAL RECESSION ( 19 FDA reports)
HAEMATURIA ( 19 FDA reports)
HYPERHIDROSIS ( 19 FDA reports)
LOSS OF CONSCIOUSNESS ( 19 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 19 FDA reports)
OBESITY ( 19 FDA reports)
OSTEOLYSIS ( 19 FDA reports)
PYURIA ( 19 FDA reports)
ROTATOR CUFF SYNDROME ( 19 FDA reports)
TENDON DISORDER ( 19 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 19 FDA reports)
VARICOSE VEIN ( 19 FDA reports)
VENOUS INSUFFICIENCY ( 19 FDA reports)
DRUG INTERACTION ( 18 FDA reports)
FLATULENCE ( 18 FDA reports)
GINGIVAL ERYTHEMA ( 18 FDA reports)
HAEMOGLOBIN DECREASED ( 18 FDA reports)
HAND FRACTURE ( 18 FDA reports)
HEART RATE INCREASED ( 18 FDA reports)
HYPERMETABOLISM ( 18 FDA reports)
IRON DEFICIENCY ANAEMIA ( 18 FDA reports)
MOBILITY DECREASED ( 18 FDA reports)
PALPITATIONS ( 18 FDA reports)
PEPTIC ULCER ( 18 FDA reports)
RADIUS FRACTURE ( 18 FDA reports)
RENAL CYST ( 18 FDA reports)
RESPIRATORY ARREST ( 18 FDA reports)
VENTRICULAR TACHYCARDIA ( 18 FDA reports)
WEIGHT INCREASED ( 18 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 17 FDA reports)
AORTIC VALVE STENOSIS ( 17 FDA reports)
ASPIRATION ( 17 FDA reports)
CANDIDIASIS ( 17 FDA reports)
COAGULOPATHY ( 17 FDA reports)
DIVERTICULUM INTESTINAL ( 17 FDA reports)
DRUG DEPENDENCE ( 17 FDA reports)
DRUG HYPERSENSITIVITY ( 17 FDA reports)
EAR CONGESTION ( 17 FDA reports)
GLOSSITIS ( 17 FDA reports)
ILEUS ( 17 FDA reports)
INCREASED TENDENCY TO BRUISE ( 17 FDA reports)
LEUKOPENIA ( 17 FDA reports)
MOUTH ULCERATION ( 17 FDA reports)
MULTIPLE MYELOMA ( 17 FDA reports)
SPEECH DISORDER ( 17 FDA reports)
STREPTOCOCCAL INFECTION ( 17 FDA reports)
TOOTH LOSS ( 17 FDA reports)
ULCER ( 17 FDA reports)
WHEEZING ( 17 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 16 FDA reports)
ACUTE SINUSITIS ( 16 FDA reports)
AMNESIA ( 16 FDA reports)
ATRIAL SEPTAL DEFECT ( 16 FDA reports)
CHEST DISCOMFORT ( 16 FDA reports)
ENCEPHALOPATHY ( 16 FDA reports)
GINGIVITIS ( 16 FDA reports)
GOITRE ( 16 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 16 FDA reports)
MASS ( 16 FDA reports)
MEMORY IMPAIRMENT ( 16 FDA reports)
METASTASES TO LIVER ( 16 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 16 FDA reports)
NEOPLASM PROGRESSION ( 16 FDA reports)
NEPHROLITHIASIS ( 16 FDA reports)
OESOPHAGITIS ( 16 FDA reports)
PLEURITIC PAIN ( 16 FDA reports)
SPINAL COLUMN STENOSIS ( 16 FDA reports)
SPINAL CORD COMPRESSION ( 16 FDA reports)
SPINAL DEFORMITY ( 16 FDA reports)
SPINAL DISORDER ( 16 FDA reports)
VITAMIN D DECREASED ( 16 FDA reports)
ACCIDENTAL OVERDOSE ( 15 FDA reports)
AGITATION ( 15 FDA reports)
BLADDER CYST ( 15 FDA reports)
BONE DENSITY DECREASED ( 15 FDA reports)
CATARACT ( 15 FDA reports)
DEHYDRATION ( 15 FDA reports)
DISTURBANCE IN ATTENTION ( 15 FDA reports)
DRUG TOXICITY ( 15 FDA reports)
LEUKOCYTOSIS ( 15 FDA reports)
MITRAL VALVE PROLAPSE ( 15 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 15 FDA reports)
ORAL DISORDER ( 15 FDA reports)
PETECHIAE ( 15 FDA reports)
PLEURAL FIBROSIS ( 15 FDA reports)
PRIMARY SEQUESTRUM ( 15 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 15 FDA reports)
RHINITIS ALLERGIC ( 15 FDA reports)
SEBORRHOEIC KERATOSIS ( 15 FDA reports)
SNORING ( 15 FDA reports)
SOMNOLENCE ( 15 FDA reports)
STEM CELL TRANSPLANT ( 15 FDA reports)
TOOTH DISORDER ( 15 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 15 FDA reports)
ABASIA ( 14 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 14 FDA reports)
ANOGENITAL WARTS ( 14 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 14 FDA reports)
BLOOD GLUCOSE INCREASED ( 14 FDA reports)
BONE ATROPHY ( 14 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 14 FDA reports)
DECUBITUS ULCER ( 14 FDA reports)
DEVICE MALFUNCTION ( 14 FDA reports)
FEMUR FRACTURE ( 14 FDA reports)
HAEMORRHAGIC ANAEMIA ( 14 FDA reports)
HYPOXIA ( 14 FDA reports)
LUMBAR RADICULOPATHY ( 14 FDA reports)
LUNG DISORDER ( 14 FDA reports)
MEDICATION ERROR ( 14 FDA reports)
MOUTH HAEMORRHAGE ( 14 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 14 FDA reports)
OTITIS MEDIA ACUTE ( 14 FDA reports)
SEASONAL ALLERGY ( 14 FDA reports)
STOMATITIS ( 14 FDA reports)
THROMBOPHLEBITIS ( 14 FDA reports)
VENOUS THROMBOSIS LIMB ( 14 FDA reports)
ACUTE RESPIRATORY FAILURE ( 13 FDA reports)
ADJUSTMENT DISORDER ( 13 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 13 FDA reports)
ANAPHYLACTIC REACTION ( 13 FDA reports)
BODY TEMPERATURE INCREASED ( 13 FDA reports)
BONE MARROW TRANSPLANT ( 13 FDA reports)
BONE NEOPLASM MALIGNANT ( 13 FDA reports)
BUNION ( 13 FDA reports)
COMA ( 13 FDA reports)
CORONARY ARTERY OCCLUSION ( 13 FDA reports)
EAR PAIN ( 13 FDA reports)
EYE INFECTION ( 13 FDA reports)
FEELING ABNORMAL ( 13 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 13 FDA reports)
HEART RATE IRREGULAR ( 13 FDA reports)
HEPATIC CYST ( 13 FDA reports)
HEPATITIS ( 13 FDA reports)
HYPERKERATOSIS ( 13 FDA reports)
HYPERTENSIVE HEART DISEASE ( 13 FDA reports)
KIDNEY INFECTION ( 13 FDA reports)
LIFE EXPECTANCY SHORTENED ( 13 FDA reports)
MENISCUS LESION ( 13 FDA reports)
PANIC DISORDER ( 13 FDA reports)
PURULENT DISCHARGE ( 13 FDA reports)
RESTLESS LEGS SYNDROME ( 13 FDA reports)
SKIN HYPERTROPHY ( 13 FDA reports)
SKIN TIGHTNESS ( 13 FDA reports)
VAGINAL INFECTION ( 13 FDA reports)
ABSCESS ( 12 FDA reports)
ACETABULUM FRACTURE ( 12 FDA reports)
BALANCE DISORDER ( 12 FDA reports)
BIPOLAR I DISORDER ( 12 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 12 FDA reports)
DIAPHRAGMATIC HERNIA ( 12 FDA reports)
DYSPHONIA ( 12 FDA reports)
DYSTONIA ( 12 FDA reports)
ECONOMIC PROBLEM ( 12 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 12 FDA reports)
FIBROSIS ( 12 FDA reports)
GALLBLADDER DISORDER ( 12 FDA reports)
HAEMANGIOMA OF LIVER ( 12 FDA reports)
HAEMOLYTIC ANAEMIA ( 12 FDA reports)
HEPATIC FAILURE ( 12 FDA reports)
HYPOAESTHESIA ORAL ( 12 FDA reports)
HYPOVENTILATION ( 12 FDA reports)
IMPULSIVE BEHAVIOUR ( 12 FDA reports)
IRRITABILITY ( 12 FDA reports)
LIGAMENT INJURY ( 12 FDA reports)
MALNUTRITION ( 12 FDA reports)
MELAENA ( 12 FDA reports)
MENOPAUSAL SYMPTOMS ( 12 FDA reports)
MUMPS ( 12 FDA reports)
MUSCULOSKELETAL DISORDER ( 12 FDA reports)
NECK INJURY ( 12 FDA reports)
NODULE ( 12 FDA reports)
OSTEORADIONECROSIS ( 12 FDA reports)
OTITIS MEDIA ( 12 FDA reports)
OVERDOSE ( 12 FDA reports)
PARANOIA ( 12 FDA reports)
PERIARTHRITIS ( 12 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 12 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 12 FDA reports)
PLATELET COUNT DECREASED ( 12 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 12 FDA reports)
PROCEDURAL PAIN ( 12 FDA reports)
RADICULOPATHY ( 12 FDA reports)
REACTIVE PSYCHOSIS ( 12 FDA reports)
RECTAL POLYP ( 12 FDA reports)
ROAD TRAFFIC ACCIDENT ( 12 FDA reports)
RUBELLA ( 12 FDA reports)
SCARLET FEVER ( 12 FDA reports)
SEDATION ( 12 FDA reports)
SINUS HEADACHE ( 12 FDA reports)
SKIN DISCOLOURATION ( 12 FDA reports)
TONSILLITIS ( 12 FDA reports)
VENA CAVA THROMBOSIS ( 12 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 11 FDA reports)
BLISTER ( 11 FDA reports)
BLOOD UREA INCREASED ( 11 FDA reports)
CARDIAC VALVE DISEASE ( 11 FDA reports)
CHEST WALL MASS ( 11 FDA reports)
CHOLECYSTITIS CHRONIC ( 11 FDA reports)
CONDITION AGGRAVATED ( 11 FDA reports)
CORNEAL DYSTROPHY ( 11 FDA reports)
DENTURE WEARER ( 11 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 11 FDA reports)
DYSGEUSIA ( 11 FDA reports)
EARLY SATIETY ( 11 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 11 FDA reports)
EYE PAIN ( 11 FDA reports)
FEELING COLD ( 11 FDA reports)
GENITAL HERPES ( 11 FDA reports)
HERPES ZOSTER ( 11 FDA reports)
HISTOPLASMOSIS ( 11 FDA reports)
HYPERGLYCAEMIA ( 11 FDA reports)
HYPERTONIC BLADDER ( 11 FDA reports)
HYPOACUSIS ( 11 FDA reports)
HYPOMANIA ( 11 FDA reports)
ILIUM FRACTURE ( 11 FDA reports)
IRRITABLE BOWEL SYNDROME ( 11 FDA reports)
MAJOR DEPRESSION ( 11 FDA reports)
NEURALGIA ( 11 FDA reports)
NEURODERMATITIS ( 11 FDA reports)
ORAL HERPES ( 11 FDA reports)
PELVIC PAIN ( 11 FDA reports)
PROTEINURIA ( 11 FDA reports)
SPLENIC LESION ( 11 FDA reports)
SYNOVITIS ( 11 FDA reports)
TENOSYNOVITIS STENOSANS ( 11 FDA reports)
TOBACCO ABUSE ( 11 FDA reports)
TONGUE ULCERATION ( 11 FDA reports)
TYPE 2 DIABETES MELLITUS ( 11 FDA reports)
URETHRAL STENOSIS ( 11 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 10 FDA reports)
ANGINA PECTORIS ( 10 FDA reports)
BACTERAEMIA ( 10 FDA reports)
BONE GRAFT ( 10 FDA reports)
BREAST CANCER ( 10 FDA reports)
BRONCHOSPASM ( 10 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 10 FDA reports)
CARDIAC TAMPONADE ( 10 FDA reports)
CEREBRAL ATROPHY ( 10 FDA reports)
COGNITIVE DISORDER ( 10 FDA reports)
COLITIS ( 10 FDA reports)
DENTAL IMPLANTATION ( 10 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 10 FDA reports)
DRUG TOLERANCE ( 10 FDA reports)
ELECTROLYTE IMBALANCE ( 10 FDA reports)
ESSENTIAL HYPERTENSION ( 10 FDA reports)
FEBRILE NEUTROPENIA ( 10 FDA reports)
HAEMODYNAMIC INSTABILITY ( 10 FDA reports)
HYPERAESTHESIA ( 10 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 10 FDA reports)
METATARSUS PRIMUS VARUS ( 10 FDA reports)
MYALGIA ( 10 FDA reports)
MYELODYSPLASTIC SYNDROME ( 10 FDA reports)
PHYSICAL DISABILITY ( 10 FDA reports)
SPINAL FUSION SURGERY ( 10 FDA reports)
UPPER LIMB FRACTURE ( 10 FDA reports)
UTERINE HAEMORRHAGE ( 10 FDA reports)
UTERINE POLYP ( 10 FDA reports)
VERTIGO ( 10 FDA reports)
WOUND SECRETION ( 10 FDA reports)
ABSCESS JAW ( 9 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 9 FDA reports)
ALVEOLAR OSTEITIS ( 9 FDA reports)
AORTIC ANEURYSM ( 9 FDA reports)
CATARACT NUCLEAR ( 9 FDA reports)
DELIRIUM ( 9 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 9 FDA reports)
DIALYSIS ( 9 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 9 FDA reports)
DYSURIA ( 9 FDA reports)
FACIAL PAIN ( 9 FDA reports)
FISTULA ( 9 FDA reports)
FLANK PAIN ( 9 FDA reports)
FLUID RETENTION ( 9 FDA reports)
HYPERCHOLESTEROLAEMIA ( 9 FDA reports)
HYPERKALAEMIA ( 9 FDA reports)
HYPOVOLAEMIA ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 9 FDA reports)
INTERSTITIAL LUNG DISEASE ( 9 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 9 FDA reports)
JAUNDICE ( 9 FDA reports)
METABOLIC ACIDOSIS ( 9 FDA reports)
NEUTROPENIA ( 9 FDA reports)
PERIODONTITIS ( 9 FDA reports)
PROCEDURAL COMPLICATION ( 9 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 9 FDA reports)
PSYCHOLOGICAL TRAUMA ( 9 FDA reports)
PULMONARY HYPERTENSION ( 9 FDA reports)
RIB FRACTURE ( 9 FDA reports)
SKIN ULCER ( 9 FDA reports)
UTERINE LEIOMYOMA ( 9 FDA reports)
ANGIOEDEMA ( 8 FDA reports)
ANOREXIA ( 8 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 8 FDA reports)
ASTIGMATISM ( 8 FDA reports)
BLADDER PROLAPSE ( 8 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 8 FDA reports)
BONE FRAGMENTATION ( 8 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 8 FDA reports)
CARDIOMYOPATHY ( 8 FDA reports)
CHOLECYSTITIS ( 8 FDA reports)
CYST ( 8 FDA reports)
CYSTITIS INTERSTITIAL ( 8 FDA reports)
DENTAL OPERATION ( 8 FDA reports)
DENTAL PLAQUE ( 8 FDA reports)
DERMATITIS ( 8 FDA reports)
DISCOMFORT ( 8 FDA reports)
DISEASE PROGRESSION ( 8 FDA reports)
DYSAESTHESIA ( 8 FDA reports)
DYSARTHRIA ( 8 FDA reports)
ENDOCARDITIS ( 8 FDA reports)
ERECTILE DYSFUNCTION ( 8 FDA reports)
GANGRENE ( 8 FDA reports)
HAEMATOCRIT DECREASED ( 8 FDA reports)
HAEMODIALYSIS ( 8 FDA reports)
HYPERSOMNIA ( 8 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 8 FDA reports)
INFUSION RELATED REACTION ( 8 FDA reports)
INTESTINAL ISCHAEMIA ( 8 FDA reports)
LYMPHADENITIS ( 8 FDA reports)
LYMPHOMA ( 8 FDA reports)
NAIL DISORDER ( 8 FDA reports)
PERIODONTAL DISEASE ( 8 FDA reports)
RASH MACULO-PAPULAR ( 8 FDA reports)
RASH PRURITIC ( 8 FDA reports)
RENAL TUBULAR NECROSIS ( 8 FDA reports)
RESPIRATORY DISORDER ( 8 FDA reports)
SCAPULA FRACTURE ( 8 FDA reports)
SKELETAL INJURY ( 8 FDA reports)
SKIN HYPERPIGMENTATION ( 8 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 8 FDA reports)
TOOTH INFECTION ( 8 FDA reports)
WALKING AID USER ( 8 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 8 FDA reports)
WOUND INFECTION ( 8 FDA reports)
ACTINIC KERATOSIS ( 7 FDA reports)
APHASIA ( 7 FDA reports)
BILIARY DILATATION ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 7 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 7 FDA reports)
BRUXISM ( 7 FDA reports)
BUTTOCK PAIN ( 7 FDA reports)
CEREBRAL HAEMORRHAGE ( 7 FDA reports)
CHOLECYSTECTOMY ( 7 FDA reports)
CIRCULATORY COLLAPSE ( 7 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 7 FDA reports)
DEMENTIA ( 7 FDA reports)
DUODENAL STENOSIS ( 7 FDA reports)
EMPHYSEMA ( 7 FDA reports)
ENDOMETRIAL DISORDER ( 7 FDA reports)
EROSIVE OESOPHAGITIS ( 7 FDA reports)
FAILURE TO THRIVE ( 7 FDA reports)
GASTRIC ULCER ( 7 FDA reports)
GENERALISED OEDEMA ( 7 FDA reports)
GRANULOMA ( 7 FDA reports)
HEPATIC LESION ( 7 FDA reports)
HERNIA ( 7 FDA reports)
HYPOTHYROIDISM ( 7 FDA reports)
IMPAIRED WORK ABILITY ( 7 FDA reports)
ISCHAEMIC HEPATITIS ( 7 FDA reports)
JOINT SPRAIN ( 7 FDA reports)
METABOLIC ENCEPHALOPATHY ( 7 FDA reports)
MICTURITION URGENCY ( 7 FDA reports)
MITRAL VALVE DISEASE ( 7 FDA reports)
MOVEMENT DISORDER ( 7 FDA reports)
MUSCLE ATROPHY ( 7 FDA reports)
NERVOUS SYSTEM DISORDER ( 7 FDA reports)
OPEN WOUND ( 7 FDA reports)
PAINFUL DEFAECATION ( 7 FDA reports)
POSTOPERATIVE INFECTION ( 7 FDA reports)
PROSTATE CANCER METASTATIC ( 7 FDA reports)
PROTHROMBIN TIME PROLONGED ( 7 FDA reports)
PYELONEPHRITIS ( 7 FDA reports)
RASH PAPULAR ( 7 FDA reports)
RECTAL FISSURE ( 7 FDA reports)
SICK SINUS SYNDROME ( 7 FDA reports)
SPINAL COMPRESSION FRACTURE ( 7 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 7 FDA reports)
TACHYPNOEA ( 7 FDA reports)
TEMPERATURE INTOLERANCE ( 7 FDA reports)
VERTEBROPLASTY ( 7 FDA reports)
VIRAL INFECTION ( 7 FDA reports)
ACUTE PULMONARY OEDEMA ( 6 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 6 FDA reports)
ANEURYSM ( 6 FDA reports)
ANIMAL BITE ( 6 FDA reports)
ANOXIC ENCEPHALOPATHY ( 6 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 6 FDA reports)
APPENDICECTOMY ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 6 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 6 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 6 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 6 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 6 FDA reports)
BLOOD SODIUM DECREASED ( 6 FDA reports)
BRACHIAL PLEXOPATHY ( 6 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 6 FDA reports)
CATHETER PLACEMENT ( 6 FDA reports)
CERVICOBRACHIAL SYNDROME ( 6 FDA reports)
COLON NEOPLASM ( 6 FDA reports)
CROHN'S DISEASE ( 6 FDA reports)
DEBRIDEMENT ( 6 FDA reports)
DEFAECATION URGENCY ( 6 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 6 FDA reports)
DEVELOPMENTAL DELAY ( 6 FDA reports)
DIVERTICULITIS ( 6 FDA reports)
DRY SKIN ( 6 FDA reports)
EDENTULOUS ( 6 FDA reports)
EPILEPSY ( 6 FDA reports)
ERYTHEMA INFECTIOSUM ( 6 FDA reports)
GALLBLADDER ENLARGEMENT ( 6 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 6 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 6 FDA reports)
HEART DISEASE CONGENITAL ( 6 FDA reports)
HEART RATE DECREASED ( 6 FDA reports)
HIP ARTHROPLASTY ( 6 FDA reports)
HYDRONEPHROSIS ( 6 FDA reports)
HYPERCALCAEMIA ( 6 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 6 FDA reports)
INTESTINAL ULCER ( 6 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 6 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 6 FDA reports)
KLEBSIELLA INFECTION ( 6 FDA reports)
KNEE ARTHROPLASTY ( 6 FDA reports)
LIP SWELLING ( 6 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 6 FDA reports)
LUNG HYPERINFLATION ( 6 FDA reports)
LUNG NEOPLASM MALIGNANT ( 6 FDA reports)
METABOLIC ALKALOSIS ( 6 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 6 FDA reports)
NASAL CONGESTION ( 6 FDA reports)
OCCULT BLOOD POSITIVE ( 6 FDA reports)
OLIGURIA ( 6 FDA reports)
ONYCHOMYCOSIS ( 6 FDA reports)
ORAL SURGERY ( 6 FDA reports)
PANCREATIC ATROPHY ( 6 FDA reports)
PANCREATIC NEOPLASM ( 6 FDA reports)
PERICARDIAL HAEMORRHAGE ( 6 FDA reports)
PERIPHERAL ISCHAEMIA ( 6 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 6 FDA reports)
PERITONITIS ( 6 FDA reports)
PITUITARY TUMOUR BENIGN ( 6 FDA reports)
PLANTAR FASCIITIS ( 6 FDA reports)
PNEUMONIA ASPIRATION ( 6 FDA reports)
POLYP ( 6 FDA reports)
POST PROCEDURAL INFECTION ( 6 FDA reports)
PROCEDURAL HYPOTENSION ( 6 FDA reports)
PROTEIN S DEFICIENCY ( 6 FDA reports)
RADIOTHERAPY ( 6 FDA reports)
RASH ERYTHEMATOUS ( 6 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 6 FDA reports)
RENAL ATROPHY ( 6 FDA reports)
RENAL INFARCT ( 6 FDA reports)
SENSATION OF PRESSURE ( 6 FDA reports)
SKIN INDURATION ( 6 FDA reports)
SKIN INJURY ( 6 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 6 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 6 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 6 FDA reports)
THYROID DISORDER ( 6 FDA reports)
TRAUMATIC HAEMATOMA ( 6 FDA reports)
UNDERWEIGHT ( 6 FDA reports)
VAGINAL HAEMORRHAGE ( 6 FDA reports)
VENOUS STENOSIS ( 6 FDA reports)
VENTRICULAR FIBRILLATION ( 6 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
ABDOMINAL PAIN LOWER ( 5 FDA reports)
ABSCESS DRAINAGE ( 5 FDA reports)
ACIDOSIS ( 5 FDA reports)
ADRENAL INSUFFICIENCY ( 5 FDA reports)
ADVERSE REACTION ( 5 FDA reports)
ANASTOMOTIC LEAK ( 5 FDA reports)
ANKLE FRACTURE ( 5 FDA reports)
ASPIRATION PLEURAL CAVITY ( 5 FDA reports)
AZOTAEMIA ( 5 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 5 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 5 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 5 FDA reports)
BLOOD TESTOSTERONE FREE DECREASED ( 5 FDA reports)
BODY HEIGHT DECREASED ( 5 FDA reports)
BONE FORMATION INCREASED ( 5 FDA reports)
BRAIN DEATH ( 5 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 5 FDA reports)
BREATH SOUNDS ABNORMAL ( 5 FDA reports)
BRONCHIAL NEOPLASM ( 5 FDA reports)
CATARACT OPERATION ( 5 FDA reports)
CHOLECYSTITIS INFECTIVE ( 5 FDA reports)
COLONIC OBSTRUCTION ( 5 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 5 FDA reports)
CYANOSIS ( 5 FDA reports)
DECREASED ACTIVITY ( 5 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
DYSKINESIA ( 5 FDA reports)
EXCORIATION ( 5 FDA reports)
FACE OEDEMA ( 5 FDA reports)
FAECALOMA ( 5 FDA reports)
FEELING HOT AND COLD ( 5 FDA reports)
FOETAL HEART RATE DECELERATION ( 5 FDA reports)
GASTROENTERITIS ( 5 FDA reports)
HYPERNATRAEMIA ( 5 FDA reports)
HYPOMAGNESAEMIA ( 5 FDA reports)
INADEQUATE ANALGESIA ( 5 FDA reports)
INJECTION SITE PAIN ( 5 FDA reports)
JAW LESION EXCISION ( 5 FDA reports)
JOINT CONTRACTURE ( 5 FDA reports)
JOINT STIFFNESS ( 5 FDA reports)
LACUNAR INFARCTION ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
LOCALISED OEDEMA ( 5 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 5 FDA reports)
MALOCCLUSION ( 5 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 5 FDA reports)
MEDIASTINAL DISORDER ( 5 FDA reports)
METASTASES TO SKIN ( 5 FDA reports)
MUCOSAL INFLAMMATION ( 5 FDA reports)
MUSCLE CRAMP ( 5 FDA reports)
NEPHROPATHY ( 5 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 5 FDA reports)
ORAL CANDIDIASIS ( 5 FDA reports)
OROPHARYNGEAL PAIN ( 5 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 5 FDA reports)
PHARYNGEAL OEDEMA ( 5 FDA reports)
PHIMOSIS ( 5 FDA reports)
PHOTOPHOBIA ( 5 FDA reports)
PHOTOPSIA ( 5 FDA reports)
PNEUMONIA BACTERIAL ( 5 FDA reports)
POST PROCEDURAL CELLULITIS ( 5 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 5 FDA reports)
PRURITUS GENERALISED ( 5 FDA reports)
PULMONARY VALVE STENOSIS ( 5 FDA reports)
QUALITY OF LIFE DECREASED ( 5 FDA reports)
RALES ( 5 FDA reports)
RESPIRATORY DEPRESSION ( 5 FDA reports)
RESTLESSNESS ( 5 FDA reports)
RETINAL TEAR ( 5 FDA reports)
SEROMA ( 5 FDA reports)
SHOCK ( 5 FDA reports)
SINUS ARRHYTHMIA ( 5 FDA reports)
SINUS BRADYCARDIA ( 5 FDA reports)
SINUS OPERATION ( 5 FDA reports)
SKIN CANCER ( 5 FDA reports)
SKIN NECROSIS ( 5 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 5 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 5 FDA reports)
SWOLLEN TONGUE ( 5 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 5 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 5 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
TOOTH FRACTURE ( 5 FDA reports)
TOOTH IMPACTED ( 5 FDA reports)
TOXIC ENCEPHALOPATHY ( 5 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
URETERIC OBSTRUCTION ( 5 FDA reports)
URINE OUTPUT DECREASED ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 4 FDA reports)
ADVERSE DRUG REACTION ( 4 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ANGINA UNSTABLE ( 4 FDA reports)
AORTIC STENOSIS ( 4 FDA reports)
ARTERIAL THROMBOSIS ( 4 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 4 FDA reports)
ARTHRITIS INFECTIVE ( 4 FDA reports)
ATRIAL FLUTTER ( 4 FDA reports)
BLINDNESS ( 4 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 4 FDA reports)
BONE TRIMMING ( 4 FDA reports)
BREAST RECONSTRUCTION ( 4 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 4 FDA reports)
BUNION OPERATION ( 4 FDA reports)
CACHEXIA ( 4 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 4 FDA reports)
CEREBRAL ISCHAEMIA ( 4 FDA reports)
CERVICAL DYSPLASIA ( 4 FDA reports)
CHOLECYSTITIS ACUTE ( 4 FDA reports)
COMPARTMENT SYNDROME ( 4 FDA reports)
CRYING ( 4 FDA reports)
CYSTOCELE ( 4 FDA reports)
DRUG ABUSER ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
ECCHYMOSIS ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 4 FDA reports)
EMBOLIC STROKE ( 4 FDA reports)
ENDODONTIC PROCEDURE ( 4 FDA reports)
GLYCOSURIA ( 4 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 4 FDA reports)
HAEMORRHAGIC STROKE ( 4 FDA reports)
HEPATOMEGALY ( 4 FDA reports)
HEPATOTOXICITY ( 4 FDA reports)
HYPERTHERMIA MALIGNANT ( 4 FDA reports)
ILL-DEFINED DISORDER ( 4 FDA reports)
INJECTION SITE HAEMATOMA ( 4 FDA reports)
INTRACRANIAL HYPOTENSION ( 4 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 4 FDA reports)
IRON DEFICIENCY ( 4 FDA reports)
JOINT DISLOCATION ( 4 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 4 FDA reports)
LEFT ATRIAL DILATATION ( 4 FDA reports)
LEUKAEMIA ( 4 FDA reports)
LIGAMENT RUPTURE ( 4 FDA reports)
LIVEDO RETICULARIS ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
MITRAL VALVE CALCIFICATION ( 4 FDA reports)
MIXED LIVER INJURY ( 4 FDA reports)
MOOD SWINGS ( 4 FDA reports)
MULTIPLE INJURIES ( 4 FDA reports)
NEPHROGENIC ANAEMIA ( 4 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
OEDEMA MUCOSAL ( 4 FDA reports)
PALLOR ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PERIORBITAL OEDEMA ( 4 FDA reports)
PERITONITIS BACTERIAL ( 4 FDA reports)
PNEUMONITIS ( 4 FDA reports)
POST-TRAUMATIC PAIN ( 4 FDA reports)
POSTOPERATIVE ILEUS ( 4 FDA reports)
PRESYNCOPE ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
PULSE ABSENT ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RECTOCELE ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
SENSORY DISTURBANCE ( 4 FDA reports)
SEROSITIS ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
STASIS DERMATITIS ( 4 FDA reports)
SUDDEN DEATH ( 4 FDA reports)
TENDON RUPTURE ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
THERAPY NON-RESPONDER ( 4 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
VITREOUS FLOATERS ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
WISDOM TEETH REMOVAL ( 4 FDA reports)
WOUND DRAINAGE ( 4 FDA reports)
X-RAY ABNORMAL ( 4 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 3 FDA reports)
ACTINOMYCOSIS ( 3 FDA reports)
ADENOCARCINOMA ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
AORTIC VALVE DISEASE ( 3 FDA reports)
AORTIC VALVE SCLEROSIS ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
ARTERIAL DISORDER ( 3 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
ASBESTOSIS ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
BILIARY DYSKINESIA ( 3 FDA reports)
BILIARY SEPSIS ( 3 FDA reports)
BLADDER CANCER ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD CREATININE DECREASED ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD DISORDER ( 3 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BRAIN DAMAGE ( 3 FDA reports)
BRAIN HERNIATION ( 3 FDA reports)
BREAKTHROUGH PAIN ( 3 FDA reports)
BREAST MASS ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CEREBRAL CALCIFICATION ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CHEST TUBE INSERTION ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CHONDROPATHY ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
CLOSTRIDIUM COLITIS ( 3 FDA reports)
COAGULATION TIME ABNORMAL ( 3 FDA reports)
COLITIS ULCERATIVE ( 3 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 3 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 3 FDA reports)
DEAFNESS BILATERAL ( 3 FDA reports)
DEVICE MISUSE ( 3 FDA reports)
DIABETIC NEUROPATHY ( 3 FDA reports)
DIASTOLIC DYSFUNCTION ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DUPUYTREN'S CONTRACTURE ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
EFFUSION ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
ESCHERICHIA BACTERAEMIA ( 3 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 3 FDA reports)
EXFOLIATIVE RASH ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
EYE ROLLING ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 3 FDA reports)
GALLBLADDER INJURY ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GINGIVAL DISORDER ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 3 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 3 FDA reports)
GOUT ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HEART VALVE INCOMPETENCE ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HIP SURGERY ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
HYPOTHERMIA ( 3 FDA reports)
IMPAIRED DRIVING ABILITY ( 3 FDA reports)
INFUSION SITE ERYTHEMA ( 3 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
ISCHAEMIC ULCER ( 3 FDA reports)
JAW DISORDER ( 3 FDA reports)
JAW OPERATION ( 3 FDA reports)
JOINT LOCK ( 3 FDA reports)
KIDNEY MALFORMATION ( 3 FDA reports)
KLEBSIELLA SEPSIS ( 3 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
LIGAMENT SPRAIN ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
MALLORY-WEISS SYNDROME ( 3 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
MEDICAL DEVICE COMPLICATION ( 3 FDA reports)
MEDICAL DIET ( 3 FDA reports)
METABOLIC DISORDER ( 3 FDA reports)
METASTASES TO LYMPH NODES ( 3 FDA reports)
MONOPLEGIA ( 3 FDA reports)
MUSCLE CONTRACTURE ( 3 FDA reports)
MUSCLE TWITCHING ( 3 FDA reports)
MYELOMALACIA ( 3 FDA reports)
MYELOPATHY ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
MYOPIA ( 3 FDA reports)
NERVE COMPRESSION ( 3 FDA reports)
NEUROMYOPATHY ( 3 FDA reports)
NODAL RHYTHM ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
ONYCHOMADESIS ( 3 FDA reports)
OPEN REDUCTION OF FRACTURE ( 3 FDA reports)
ORAL INTAKE REDUCED ( 3 FDA reports)
ORTHOPNOEA ( 3 FDA reports)
OSTEOMYELITIS CHRONIC ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PLATELET COUNT ABNORMAL ( 3 FDA reports)
PLEURAL DECORTICATION ( 3 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 3 FDA reports)
PORTAL VEIN THROMBOSIS ( 3 FDA reports)
POST PROCEDURAL DISCHARGE ( 3 FDA reports)
POST PROCEDURAL HAEMATOMA ( 3 FDA reports)
POST-TRAUMATIC HEADACHE ( 3 FDA reports)
PRESBYOPIA ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
RADIATION FIBROSIS ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
RENAL CELL CARCINOMA ( 3 FDA reports)
RENAL DYSPLASIA ( 3 FDA reports)
RENAL MASS ( 3 FDA reports)
RESPIRATORY RATE DECREASED ( 3 FDA reports)
RESPIRATORY RATE INCREASED ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
RHINORRHOEA ( 3 FDA reports)
RIGHT ATRIAL DILATATION ( 3 FDA reports)
SENSORY LOSS ( 3 FDA reports)
SERRATIA SEPSIS ( 3 FDA reports)
SHOULDER ARTHROPLASTY ( 3 FDA reports)
SKIN FIBROSIS ( 3 FDA reports)
SKIN WRINKLING ( 3 FDA reports)
SOFT TISSUE INFECTION ( 3 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
STATUS MIGRAINOSUS ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
TARDIVE DYSKINESIA ( 3 FDA reports)
TENSION HEADACHE ( 3 FDA reports)
THIRST ( 3 FDA reports)
THORACOSTOMY ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
THYROID NEOPLASM ( 3 FDA reports)
TOE AMPUTATION ( 3 FDA reports)
TOXIC ANTERIOR SEGMENT SYNDROME ( 3 FDA reports)
TRANSFUSION ( 3 FDA reports)
TROPONIN I INCREASED ( 3 FDA reports)
TYPE 1 DIABETES MELLITUS ( 3 FDA reports)
URINARY HESITATION ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
URINE ANALYSIS ABNORMAL ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
WOUND INFECTION BACTERIAL ( 3 FDA reports)
WRIST FRACTURE ( 3 FDA reports)
ABDOMINAL INFECTION ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ACUTE PRERENAL FAILURE ( 2 FDA reports)
ADENOMA BENIGN ( 2 FDA reports)
ADHESION ( 2 FDA reports)
ADNEXA UTERI CYST ( 2 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 2 FDA reports)
ALLERGIC SINUSITIS ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANGER ( 2 FDA reports)
AORTIC DISORDER ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
APNOEA ( 2 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 2 FDA reports)
ARTHRITIS BACTERIAL ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
AUTOMATISM ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BILIARY COLIC ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BITE ( 2 FDA reports)
BLADDER SPASM ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 2 FDA reports)
BLOODY DISCHARGE ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BREAST CALCIFICATIONS ( 2 FDA reports)
BREAST CYST ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 2 FDA reports)
CARDIAC PERFORATION ( 2 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CEREBELLAR ATROPHY ( 2 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 2 FDA reports)
CEREBROSPINAL FISTULA ( 2 FDA reports)
CERUMEN IMPACTION ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CLEFT LIP ( 2 FDA reports)
CLEFT PALATE ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
CONJUNCTIVOCHALASIS ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
CORNEAL OPACITY ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
CYSTOSTOMY ( 2 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DEVICE DISLOCATION ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DRY GANGRENE ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
ECHOLALIA ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 2 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FAT EMBOLISM ( 2 FDA reports)
FIBRIN D DIMER ( 2 FDA reports)
FIBROADENOMA OF BREAST ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
GLARE ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GRAFT HAEMORRHAGE ( 2 FDA reports)
HAEMANGIOMA ( 2 FDA reports)
HAEMARTHROSIS ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEMIANOPIA ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC MASS ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HILAR LYMPHADENOPATHY ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYDROPNEUMOTHORAX ( 2 FDA reports)
HYPERPHAGIA ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 2 FDA reports)
HYPOPERFUSION ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
HYSTERECTOMY ( 2 FDA reports)
ILEITIS ( 2 FDA reports)
INCISION SITE COMPLICATION ( 2 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 2 FDA reports)
INFLAMMATORY PAIN ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INGROWING NAIL ( 2 FDA reports)
INTERNAL INJURY ( 2 FDA reports)
INTERTRIGO ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
JOINT CREPITATION ( 2 FDA reports)
LABILE BLOOD PRESSURE ( 2 FDA reports)
LACTOSE INTOLERANCE ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LOOSE BODY IN JOINT ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 2 FDA reports)
MELANOSIS COLI ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
METASTASES TO PERITONEUM ( 2 FDA reports)
METASTATIC GASTRIC CANCER ( 2 FDA reports)
MICROANGIOPATHY ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 2 FDA reports)
ORAL DISCOMFORT ( 2 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PELVIC HAEMATOMA ( 2 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 2 FDA reports)
PERITONEAL HAEMORRHAGE ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
POLYMYOSITIS ( 2 FDA reports)
POST PROCEDURAL NAUSEA ( 2 FDA reports)
POST PROCEDURAL VOMITING ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PROPIONIBACTERIUM INFECTION ( 2 FDA reports)
PULMONARY EOSINOPHILIA ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
PURULENCE ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
RENAL ARTERY THROMBOSIS ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
REPETITIVE STRAIN INJURY ( 2 FDA reports)
RESORPTION BONE INCREASED ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
ROTATOR CUFF REPAIR ( 2 FDA reports)
SCAB ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SKIN SWELLING ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SOFT TISSUE DISORDER ( 2 FDA reports)
SPLEEN CONGESTION ( 2 FDA reports)
SPLENIC GRANULOMA ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
SUTURE RELATED COMPLICATION ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
TACHYCARDIA FOETAL ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
TENDON GRAFT ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TONSILLAR DISORDER ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 2 FDA reports)
TRAUMATIC ARTHRITIS ( 2 FDA reports)
TUBO-OVARIAN ABSCESS ( 2 FDA reports)
ULNAR NEURITIS ( 2 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 2 FDA reports)
URINARY BLADDER POLYP ( 2 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 2 FDA reports)
VARICOSE ULCERATION ( 2 FDA reports)
VASCULAR CALCIFICATION ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 2 FDA reports)
WEIGHT ABNORMAL ( 2 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 2 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ADAMS-STOKES SYNDROME ( 1 FDA reports)
AIRWAY PEAK PRESSURE INCREASED ( 1 FDA reports)
ALVEOLOPLASTY ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC EMBOLUS ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTHROFIBROSIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
AURA ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 1 FDA reports)
BLOODY AIRWAY DISCHARGE ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE CYST ( 1 FDA reports)
BONE OPERATION ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST HAEMORRHAGE ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BURSA REMOVAL ( 1 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC PACEMAKER REVISION ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLESTEROSIS ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONFUSION POSTOPERATIVE ( 1 FDA reports)
CONGENITAL AORTIC ANOMALY ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONTRAST MEDIA ALLERGY ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DENTAL PULP DISORDER ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROCOLONIC FISTULA ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE INFECTION VIRAL ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
GALLBLADDER OBSTRUCTION ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GESTATIONAL HYPERTENSION ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAFT LOSS ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HAND AMPUTATION ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEREDITARY SPHEROCYTOSIS ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIDRADENITIS ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IDIOPATHIC URTICARIA ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMPLANT SITE CELLULITIS ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCISION SITE CELLULITIS ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE DISCHARGE ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERCOSTAL RETRACTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
IRON OVERLOAD ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT ADHESION ( 1 FDA reports)
JOINT DEPOSIT ( 1 FDA reports)
JOINT DESTRUCTION ( 1 FDA reports)
JOINT HYPEREXTENSION ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
KNEE IMPINGEMENT SYNDROME ( 1 FDA reports)
KYPHOSIS ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LATENT SYPHILIS ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LIGAMENT LAXITY ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG WEDGE RESECTION ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 1 FDA reports)
MEDICAL DEVICE REMOVAL ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MITOCHONDRIAL DNA MUTATION ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCLE GRAFT ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEONATAL RESPIRATORY DEPRESSION ( 1 FDA reports)
NEONATAL TACHYPNOEA ( 1 FDA reports)
NEOPLASM GROWTH ACCELERATED ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OCULOGYRATION ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
ONYCHALGIA ( 1 FDA reports)
ORAL CAVITY FISTULA ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 1 FDA reports)
PERICARDIAL DRAINAGE ( 1 FDA reports)
PERICARDIAL RUB ( 1 FDA reports)
PERIPHERAL NERVE DESTRUCTION ( 1 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 1 FDA reports)
PHLEBOLITH ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREOPERATIVE CARE ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PRODUCT CONTAMINATION PHYSICAL ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROPOFOL INFUSION SYNDROME ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RED BLOOD CELL NUCLEATED MORPHOLOGY PRESENT ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RENAL VEIN OCCLUSION ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETROPERITONEAL ABSCESS ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RIB EXCISION ( 1 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SALIVARY GLAND CANCER ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SECONDARY SYPHILIS ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPLENIC CALCIFICATION ( 1 FDA reports)
SPONDYLITIS ( 1 FDA reports)
SPONDYLOARTHROPATHY ( 1 FDA reports)
STARING ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STITCH ABSCESS ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUBVALVULAR AORTIC STENOSIS ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TENODESIS ( 1 FDA reports)
TENSION ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THORACOTOMY ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBECTOMY ( 1 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX INCREASED ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRACHOMA ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSFUSION-TRANSMITTED INFECTIOUS DISEASE ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
UROBILINOGEN URINE INCREASED ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE ATROPHY ( 1 FDA reports)
UTERINE SPASM ( 1 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VEIN WALL HYPERTROPHY ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VISCERAL CONGESTION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND DECOMPOSITION ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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