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

PAIN ( 807 FDA reports)
ANAEMIA ( 622 FDA reports)
ANXIETY ( 616 FDA reports)
PYREXIA ( 606 FDA reports)
NAUSEA ( 573 FDA reports)
OSTEONECROSIS OF JAW ( 559 FDA reports)
BONE DISORDER ( 542 FDA reports)
DYSPNOEA ( 525 FDA reports)
PNEUMONIA ( 470 FDA reports)
INJURY ( 463 FDA reports)
VOMITING ( 454 FDA reports)
DIARRHOEA ( 453 FDA reports)
BACK PAIN ( 438 FDA reports)
OSTEONECROSIS ( 425 FDA reports)
FEBRILE NEUTROPENIA ( 400 FDA reports)
FATIGUE ( 399 FDA reports)
TOOTH EXTRACTION ( 377 FDA reports)
PAIN IN JAW ( 368 FDA reports)
ASTHENIA ( 360 FDA reports)
NEUTROPENIA ( 357 FDA reports)
ARTHRALGIA ( 343 FDA reports)
PLEURAL EFFUSION ( 339 FDA reports)
WEIGHT DECREASED ( 339 FDA reports)
THROMBOCYTOPENIA ( 333 FDA reports)
NEUROPATHY PERIPHERAL ( 326 FDA reports)
OSTEOMYELITIS ( 318 FDA reports)
INFECTION ( 317 FDA reports)
OSTEOARTHRITIS ( 294 FDA reports)
ABDOMINAL PAIN ( 291 FDA reports)
OEDEMA PERIPHERAL ( 290 FDA reports)
CHEST PAIN ( 289 FDA reports)
HEADACHE ( 286 FDA reports)
HYPOAESTHESIA ( 285 FDA reports)
PANCYTOPENIA ( 272 FDA reports)
DEPRESSION ( 267 FDA reports)
CONSTIPATION ( 261 FDA reports)
IMPAIRED HEALING ( 260 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 257 FDA reports)
DEEP VEIN THROMBOSIS ( 254 FDA reports)
BRONCHITIS ( 250 FDA reports)
ATELECTASIS ( 249 FDA reports)
FALL ( 248 FDA reports)
METASTASES TO BONE ( 247 FDA reports)
COUGH ( 244 FDA reports)
PARAESTHESIA ( 244 FDA reports)
BONE PAIN ( 242 FDA reports)
DENTAL CARIES ( 231 FDA reports)
CELLULITIS ( 229 FDA reports)
SEPSIS ( 228 FDA reports)
SINUSITIS ( 228 FDA reports)
HYPERTENSION ( 226 FDA reports)
SWELLING ( 225 FDA reports)
BONE LESION ( 224 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 219 FDA reports)
LYMPHADENOPATHY ( 216 FDA reports)
SPINAL OSTEOARTHRITIS ( 216 FDA reports)
DYSPHAGIA ( 215 FDA reports)
MUCOSAL INFLAMMATION ( 215 FDA reports)
OSTEOPENIA ( 213 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 211 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 201 FDA reports)
ANHEDONIA ( 200 FDA reports)
PAIN IN EXTREMITY ( 200 FDA reports)
DEHYDRATION ( 199 FDA reports)
DECREASED APPETITE ( 195 FDA reports)
INSOMNIA ( 195 FDA reports)
NEOPLASM MALIGNANT ( 194 FDA reports)
TOOTH DISORDER ( 193 FDA reports)
HYPOTENSION ( 190 FDA reports)
TOOTHACHE ( 179 FDA reports)
DEATH ( 178 FDA reports)
ERYTHEMA ( 176 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 175 FDA reports)
DIZZINESS ( 174 FDA reports)
GASTRITIS ( 171 FDA reports)
URINARY TRACT INFECTION ( 171 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 170 FDA reports)
HYPOKALAEMIA ( 166 FDA reports)
PRIMARY SEQUESTRUM ( 166 FDA reports)
MUSCULOSKELETAL PAIN ( 162 FDA reports)
EMOTIONAL DISTRESS ( 161 FDA reports)
GAIT DISTURBANCE ( 159 FDA reports)
NECK PAIN ( 158 FDA reports)
PLATELET COUNT DECREASED ( 157 FDA reports)
INFLAMMATION ( 156 FDA reports)
RASH ( 153 FDA reports)
COMPRESSION FRACTURE ( 152 FDA reports)
MYALGIA ( 149 FDA reports)
EAR PAIN ( 147 FDA reports)
MUSCULAR WEAKNESS ( 146 FDA reports)
OSTEOLYSIS ( 145 FDA reports)
RIB FRACTURE ( 144 FDA reports)
STAPHYLOCOCCAL INFECTION ( 144 FDA reports)
CHILLS ( 142 FDA reports)
ORAL PAIN ( 142 FDA reports)
TOOTH ABSCESS ( 141 FDA reports)
PERIODONTAL DISEASE ( 139 FDA reports)
RENAL FAILURE ( 139 FDA reports)
HERPES ZOSTER ( 138 FDA reports)
SCOLIOSIS ( 138 FDA reports)
HYPOXIA ( 137 FDA reports)
RENAL FAILURE ACUTE ( 137 FDA reports)
HIATUS HERNIA ( 135 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 135 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 134 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 133 FDA reports)
PULMONARY EMBOLISM ( 131 FDA reports)
DISEASE PROGRESSION ( 130 FDA reports)
RENAL FAILURE CHRONIC ( 130 FDA reports)
STOMATITIS ( 128 FDA reports)
MULTIPLE MYELOMA ( 127 FDA reports)
ATRIAL FIBRILLATION ( 126 FDA reports)
DECREASED INTEREST ( 126 FDA reports)
TOOTH LOSS ( 125 FDA reports)
HAEMORRHOIDS ( 124 FDA reports)
LEUKOPENIA ( 124 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 122 FDA reports)
LOOSE TOOTH ( 121 FDA reports)
METASTASES TO LIVER ( 121 FDA reports)
BURSITIS ( 120 FDA reports)
CARDIOMEGALY ( 120 FDA reports)
METASTASES TO LUNG ( 120 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 119 FDA reports)
CATARACT ( 118 FDA reports)
DEFORMITY ( 118 FDA reports)
HAEMOGLOBIN DECREASED ( 118 FDA reports)
SYNCOPE ( 118 FDA reports)
CONFUSIONAL STATE ( 117 FDA reports)
JAW OPERATION ( 117 FDA reports)
ALOPECIA ( 116 FDA reports)
DISABILITY ( 116 FDA reports)
OSTEOSCLEROSIS ( 115 FDA reports)
BONE DEBRIDEMENT ( 114 FDA reports)
FISTULA ( 114 FDA reports)
PATHOLOGICAL FRACTURE ( 114 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 110 FDA reports)
DYSPNOEA EXERTIONAL ( 110 FDA reports)
EJECTION FRACTION DECREASED ( 109 FDA reports)
SINUS DISORDER ( 109 FDA reports)
RENAL CYST ( 108 FDA reports)
OSTEOPOROSIS ( 106 FDA reports)
HYPONATRAEMIA ( 105 FDA reports)
LUNG NEOPLASM ( 105 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 105 FDA reports)
ABSCESS ( 104 FDA reports)
EXOSTOSIS ( 103 FDA reports)
PURULENT DISCHARGE ( 102 FDA reports)
WEIGHT INCREASED ( 102 FDA reports)
DRUG INEFFECTIVE ( 101 FDA reports)
HOT FLUSH ( 101 FDA reports)
HYPOPHAGIA ( 101 FDA reports)
ASTHMA ( 100 FDA reports)
METASTASES TO SPINE ( 99 FDA reports)
MITRAL VALVE INCOMPETENCE ( 99 FDA reports)
RESPIRATORY FAILURE ( 99 FDA reports)
CARDIOMYOPATHY ( 98 FDA reports)
DIVERTICULUM ( 98 FDA reports)
LUNG INFILTRATION ( 98 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 97 FDA reports)
MYOCARDIAL INFARCTION ( 97 FDA reports)
BLOOD CREATININE INCREASED ( 96 FDA reports)
BLOOD GLUCOSE INCREASED ( 96 FDA reports)
SINUS TACHYCARDIA ( 96 FDA reports)
DIVERTICULUM INTESTINAL ( 95 FDA reports)
SEPTIC SHOCK ( 95 FDA reports)
TACHYCARDIA ( 95 FDA reports)
CERVICAL SPINAL STENOSIS ( 94 FDA reports)
CONVULSION ( 94 FDA reports)
ARTHRITIS ( 93 FDA reports)
MASTICATION DISORDER ( 93 FDA reports)
COLITIS ( 92 FDA reports)
JAW DISORDER ( 92 FDA reports)
PNEUMONITIS ( 92 FDA reports)
ACTINOMYCOSIS ( 90 FDA reports)
DEBRIDEMENT ( 90 FDA reports)
DYSURIA ( 90 FDA reports)
HYPERLIPIDAEMIA ( 90 FDA reports)
MALAISE ( 90 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 90 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 89 FDA reports)
MASS ( 89 FDA reports)
GINGIVAL BLEEDING ( 88 FDA reports)
PULMONARY OEDEMA ( 88 FDA reports)
HAEMATOCHEZIA ( 87 FDA reports)
MENTAL STATUS CHANGES ( 87 FDA reports)
OSTEITIS ( 87 FDA reports)
PERICARDIAL EFFUSION ( 87 FDA reports)
ORAL INFECTION ( 86 FDA reports)
ORAL DISORDER ( 85 FDA reports)
STEM CELL TRANSPLANT ( 85 FDA reports)
HEPATIC LESION ( 84 FDA reports)
SCAR ( 84 FDA reports)
HYPERCHOLESTEROLAEMIA ( 83 FDA reports)
VISUAL IMPAIRMENT ( 83 FDA reports)
CARDIAC ARREST ( 82 FDA reports)
GINGIVAL SWELLING ( 82 FDA reports)
OROPHARYNGEAL PAIN ( 82 FDA reports)
SPINAL COMPRESSION FRACTURE ( 82 FDA reports)
SWELLING FACE ( 82 FDA reports)
ENDODONTIC PROCEDURE ( 81 FDA reports)
DYSGEUSIA ( 80 FDA reports)
HYPERKALAEMIA ( 80 FDA reports)
JAW FRACTURE ( 80 FDA reports)
MUSCLE SPASMS ( 80 FDA reports)
SYNOVIAL CYST ( 80 FDA reports)
LUNG DISORDER ( 79 FDA reports)
DYSPEPSIA ( 78 FDA reports)
GINGIVAL PAIN ( 78 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 78 FDA reports)
HYPOTHYROIDISM ( 77 FDA reports)
KYPHOSIS ( 77 FDA reports)
TOOTH FRACTURE ( 76 FDA reports)
CONTUSION ( 75 FDA reports)
ORAL CANDIDIASIS ( 75 FDA reports)
HEPATIC STEATOSIS ( 74 FDA reports)
HYPOAESTHESIA ORAL ( 74 FDA reports)
CORONARY ARTERY DISEASE ( 73 FDA reports)
MYELODYSPLASTIC SYNDROME ( 73 FDA reports)
SOFT TISSUE DISORDER ( 73 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 72 FDA reports)
HAEMATURIA ( 72 FDA reports)
NEOPLASM PROGRESSION ( 72 FDA reports)
VISION BLURRED ( 72 FDA reports)
CANDIDIASIS ( 71 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 71 FDA reports)
TENDERNESS ( 71 FDA reports)
ABSCESS JAW ( 70 FDA reports)
PHYSICAL DISABILITY ( 70 FDA reports)
TREMOR ( 70 FDA reports)
ABDOMINAL PAIN UPPER ( 69 FDA reports)
BONE MARROW FAILURE ( 69 FDA reports)
LUMBAR SPINAL STENOSIS ( 69 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 69 FDA reports)
ASCITES ( 68 FDA reports)
EMPHYSEMA ( 68 FDA reports)
GINGIVITIS ( 68 FDA reports)
NIGHT SWEATS ( 68 FDA reports)
SKIN LESION ( 68 FDA reports)
BREAST CANCER METASTATIC ( 67 FDA reports)
DENTURE WEARER ( 67 FDA reports)
PALPITATIONS ( 67 FDA reports)
TENDONITIS ( 67 FDA reports)
BLOOD CALCIUM DECREASED ( 66 FDA reports)
HYPERCALCAEMIA ( 66 FDA reports)
CEREBROVASCULAR ACCIDENT ( 65 FDA reports)
OEDEMA ( 65 FDA reports)
PULMONARY CONGESTION ( 65 FDA reports)
AGRANULOCYTOSIS ( 64 FDA reports)
BONE MARROW TRANSPLANT ( 64 FDA reports)
CARDIAC DISORDER ( 64 FDA reports)
ODYNOPHAGIA ( 64 FDA reports)
BLOOD PRESSURE INCREASED ( 63 FDA reports)
BONE DENSITY DECREASED ( 63 FDA reports)
DENTAL FISTULA ( 63 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 63 FDA reports)
PNEUMOTHORAX ( 62 FDA reports)
RECTAL HAEMORRHAGE ( 62 FDA reports)
ABDOMINAL DISCOMFORT ( 61 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 61 FDA reports)
DIABETES MELLITUS ( 61 FDA reports)
HAEMATOCRIT DECREASED ( 61 FDA reports)
NEURALGIA ( 61 FDA reports)
SLEEP APNOEA SYNDROME ( 61 FDA reports)
ABSCESS DRAINAGE ( 60 FDA reports)
ARTERIOSCLEROSIS ( 60 FDA reports)
DEVICE RELATED INFECTION ( 60 FDA reports)
EXPOSED BONE IN JAW ( 60 FDA reports)
MULTI-ORGAN FAILURE ( 60 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 59 FDA reports)
ARTHROPATHY ( 59 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 59 FDA reports)
JOINT SWELLING ( 59 FDA reports)
NASAL CONGESTION ( 59 FDA reports)
SEQUESTRECTOMY ( 59 FDA reports)
HYPERSENSITIVITY ( 58 FDA reports)
MYELOMA RECURRENCE ( 58 FDA reports)
NEPHROLITHIASIS ( 58 FDA reports)
ORAL DISCOMFORT ( 58 FDA reports)
BONE OPERATION ( 57 FDA reports)
CHOLELITHIASIS ( 57 FDA reports)
CONJUNCTIVITIS ( 57 FDA reports)
DRUG INTERACTION ( 57 FDA reports)
GINGIVAL INFECTION ( 57 FDA reports)
MIGRAINE ( 57 FDA reports)
DECUBITUS ULCER ( 56 FDA reports)
GINGIVAL DISORDER ( 56 FDA reports)
HEPATIC CYST ( 56 FDA reports)
OSTEOMYELITIS CHRONIC ( 56 FDA reports)
SPONDYLOLISTHESIS ( 56 FDA reports)
CARDIAC MURMUR ( 55 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 55 FDA reports)
CYST ( 55 FDA reports)
HIP FRACTURE ( 55 FDA reports)
PRURITUS ( 55 FDA reports)
PULMONARY FIBROSIS ( 55 FDA reports)
AMNESIA ( 54 FDA reports)
CARPAL TUNNEL SYNDROME ( 54 FDA reports)
CEREBRAL INFARCTION ( 54 FDA reports)
CHEST DISCOMFORT ( 54 FDA reports)
DENTAL OPERATION ( 54 FDA reports)
HODGKIN'S DISEASE ( 54 FDA reports)
LYMPHOEDEMA ( 54 FDA reports)
MOBILITY DECREASED ( 54 FDA reports)
UTERINE LEIOMYOMA ( 54 FDA reports)
BRUXISM ( 53 FDA reports)
HYDRONEPHROSIS ( 53 FDA reports)
HYPERGLYCAEMIA ( 53 FDA reports)
INTERSTITIAL LUNG DISEASE ( 53 FDA reports)
MALNUTRITION ( 53 FDA reports)
NEUTROPHIL COUNT DECREASED ( 53 FDA reports)
ORAL SURGERY ( 53 FDA reports)
SKIN ULCER ( 53 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 53 FDA reports)
TOOTH INFECTION ( 53 FDA reports)
URINARY INCONTINENCE ( 53 FDA reports)
BLOOD POTASSIUM DECREASED ( 52 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 52 FDA reports)
OESOPHAGITIS ( 52 FDA reports)
PULMONARY HYPERTENSION ( 52 FDA reports)
DISCOMFORT ( 51 FDA reports)
FACIAL PAIN ( 51 FDA reports)
FIBROMYALGIA ( 51 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 51 FDA reports)
PLEURAL FIBROSIS ( 51 FDA reports)
BLOOD ALBUMIN DECREASED ( 50 FDA reports)
GASTRIC POLYPS ( 50 FDA reports)
LIFE EXPECTANCY SHORTENED ( 50 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 50 FDA reports)
VIRAL INFECTION ( 50 FDA reports)
COAGULOPATHY ( 49 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 49 FDA reports)
MOUTH ULCERATION ( 49 FDA reports)
RADICULOPATHY ( 49 FDA reports)
WHEELCHAIR USER ( 49 FDA reports)
ENCEPHALOPATHY ( 48 FDA reports)
HAEMORRHAGE ( 48 FDA reports)
LOSS OF CONSCIOUSNESS ( 48 FDA reports)
METASTATIC NEOPLASM ( 48 FDA reports)
OVARIAN CYST ( 48 FDA reports)
PRODUCTIVE COUGH ( 48 FDA reports)
BREAST CANCER ( 47 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 47 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 47 FDA reports)
SURGERY ( 47 FDA reports)
THROMBOSIS ( 47 FDA reports)
DEAFNESS ( 46 FDA reports)
FLUID RETENTION ( 46 FDA reports)
GRANULOMA ( 46 FDA reports)
ABDOMINAL DISTENSION ( 45 FDA reports)
BACTERAEMIA ( 45 FDA reports)
LUNG NEOPLASM MALIGNANT ( 45 FDA reports)
PHARYNGITIS ( 45 FDA reports)
POLLAKIURIA ( 45 FDA reports)
ABDOMINAL HERNIA ( 44 FDA reports)
HEPATITIS B ( 44 FDA reports)
ILEUS ( 44 FDA reports)
SLEEP DISORDER ( 44 FDA reports)
SPINAL COLUMN STENOSIS ( 44 FDA reports)
AZOTAEMIA ( 43 FDA reports)
CHRONIC SINUSITIS ( 43 FDA reports)
GASTROINTESTINAL DISORDER ( 43 FDA reports)
KLEBSIELLA INFECTION ( 43 FDA reports)
PELVIC PAIN ( 43 FDA reports)
SARCOIDOSIS ( 43 FDA reports)
SKIN EXFOLIATION ( 43 FDA reports)
ALVEOLOPLASTY ( 42 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 42 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 42 FDA reports)
CONDITION AGGRAVATED ( 42 FDA reports)
DIPLOPIA ( 42 FDA reports)
INFLUENZA ( 42 FDA reports)
THROMBOSIS IN DEVICE ( 42 FDA reports)
BACTERIAL INFECTION ( 41 FDA reports)
BONE FRAGMENTATION ( 41 FDA reports)
CARDIO-RESPIRATORY ARREST ( 41 FDA reports)
EDENTULOUS ( 41 FDA reports)
HEPATITIS ( 41 FDA reports)
MOUTH HAEMORRHAGE ( 41 FDA reports)
SKIN DISORDER ( 41 FDA reports)
SOMNOLENCE ( 41 FDA reports)
FEELING ABNORMAL ( 40 FDA reports)
FIBROSIS ( 40 FDA reports)
LEUKOENCEPHALOPATHY ( 40 FDA reports)
OVARIAN CANCER ( 40 FDA reports)
PROTHROMBIN TIME PROLONGED ( 40 FDA reports)
VAGINAL HAEMORRHAGE ( 40 FDA reports)
WOUND DEBRIDEMENT ( 40 FDA reports)
CATARACT OPERATION ( 39 FDA reports)
DILATATION VENTRICULAR ( 39 FDA reports)
ILEUS PARALYTIC ( 39 FDA reports)
IRON DEFICIENCY ANAEMIA ( 39 FDA reports)
LEUKOCYTOSIS ( 39 FDA reports)
OTITIS EXTERNA ( 39 FDA reports)
STREPTOCOCCAL SEPSIS ( 39 FDA reports)
CARDIOTOXICITY ( 38 FDA reports)
INFLUENZA LIKE ILLNESS ( 38 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 38 FDA reports)
SKIN HYPERPIGMENTATION ( 38 FDA reports)
SKIN PAPILLOMA ( 38 FDA reports)
BLOOD SODIUM DECREASED ( 37 FDA reports)
BREAST MASS ( 37 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 37 FDA reports)
CARDIAC FAILURE ( 37 FDA reports)
CEREBRAL ATROPHY ( 37 FDA reports)
DENTAL PLAQUE ( 37 FDA reports)
EATING DISORDER ( 37 FDA reports)
ONYCHOMYCOSIS ( 37 FDA reports)
PARAESTHESIA ORAL ( 37 FDA reports)
PERIODONTITIS ( 37 FDA reports)
PROTEINURIA ( 37 FDA reports)
RASH PRURITIC ( 37 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 37 FDA reports)
RESPIRATORY TRACT INFECTION ( 37 FDA reports)
TONGUE INJURY ( 37 FDA reports)
TRANSFUSION ( 37 FDA reports)
VERTIGO ( 37 FDA reports)
EPISTAXIS ( 36 FDA reports)
HAEMOPTYSIS ( 36 FDA reports)
LACERATION ( 36 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 36 FDA reports)
RENAL IMPAIRMENT ( 36 FDA reports)
SPINAL DISORDER ( 36 FDA reports)
WOUND DEHISCENCE ( 36 FDA reports)
AORTIC VALVE INCOMPETENCE ( 35 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 35 FDA reports)
DRUG TOXICITY ( 35 FDA reports)
ENDOCARDITIS ( 35 FDA reports)
GINGIVAL EROSION ( 35 FDA reports)
LYMPHOMA ( 35 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 35 FDA reports)
SPLENOMEGALY ( 35 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 34 FDA reports)
ASEPTIC NECROSIS BONE ( 34 FDA reports)
COMA ( 34 FDA reports)
ESCHERICHIA INFECTION ( 34 FDA reports)
FLANK PAIN ( 34 FDA reports)
HEART RATE INCREASED ( 34 FDA reports)
PULMONARY TOXICITY ( 34 FDA reports)
RENAL DISORDER ( 34 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 34 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 34 FDA reports)
WHEEZING ( 34 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 33 FDA reports)
ELECTROLYTE IMBALANCE ( 33 FDA reports)
ERECTILE DYSFUNCTION ( 33 FDA reports)
FLUID OVERLOAD ( 33 FDA reports)
FUNGAL INFECTION ( 33 FDA reports)
GINGIVAL OEDEMA ( 33 FDA reports)
ORTHOSTATIC HYPOTENSION ( 33 FDA reports)
OTITIS MEDIA ( 33 FDA reports)
RESPIRATORY DISTRESS ( 33 FDA reports)
SCIATICA ( 33 FDA reports)
SEDATION ( 33 FDA reports)
SKIN DISCOLOURATION ( 33 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 33 FDA reports)
BREATH ODOUR ( 32 FDA reports)
DEAFNESS NEUROSENSORY ( 32 FDA reports)
EAR INFECTION ( 32 FDA reports)
IRRITABILITY ( 32 FDA reports)
JUGULAR VEIN THROMBOSIS ( 32 FDA reports)
RADIOTHERAPY ( 32 FDA reports)
VENOUS THROMBOSIS LIMB ( 32 FDA reports)
ACNE ( 31 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 31 FDA reports)
ASPIRATION PLEURAL CAVITY ( 31 FDA reports)
FRACTURED SACRUM ( 31 FDA reports)
GALLBLADDER DISORDER ( 31 FDA reports)
HEPATIC FAILURE ( 31 FDA reports)
JOINT STIFFNESS ( 31 FDA reports)
LUMBAR RADICULOPATHY ( 31 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 31 FDA reports)
METASTASIS ( 31 FDA reports)
NOCTURIA ( 31 FDA reports)
ROTATOR CUFF SYNDROME ( 31 FDA reports)
ULCER ( 31 FDA reports)
ARRHYTHMIA ( 30 FDA reports)
BREAST TENDERNESS ( 30 FDA reports)
EYELID OEDEMA ( 30 FDA reports)
HAEMANGIOMA ( 30 FDA reports)
HEART RATE IRREGULAR ( 30 FDA reports)
HEPATIC MASS ( 30 FDA reports)
IMMUNODEFICIENCY ( 30 FDA reports)
JOINT EFFUSION ( 30 FDA reports)
LETHARGY ( 30 FDA reports)
NASAL MUCOSAL DISORDER ( 30 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 30 FDA reports)
PLEURITIC PAIN ( 30 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 30 FDA reports)
POST HERPETIC NEURALGIA ( 30 FDA reports)
TONGUE ULCERATION ( 30 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 29 FDA reports)
BASAL CELL CARCINOMA ( 29 FDA reports)
BONE FORMATION INCREASED ( 29 FDA reports)
CERVICAL DYSPLASIA ( 29 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 29 FDA reports)
DISORIENTATION ( 29 FDA reports)
EAR DISCOMFORT ( 29 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 29 FDA reports)
HYPERPLASIA ( 29 FDA reports)
LYMPHADENECTOMY ( 29 FDA reports)
NEPHROSCLEROSIS ( 29 FDA reports)
RASH ERYTHEMATOUS ( 29 FDA reports)
RHINITIS ( 29 FDA reports)
ROAD TRAFFIC ACCIDENT ( 29 FDA reports)
SENSITIVITY OF TEETH ( 29 FDA reports)
SOFT TISSUE INFLAMMATION ( 29 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 29 FDA reports)
WOUND DRAINAGE ( 29 FDA reports)
WOUND SECRETION ( 29 FDA reports)
ADNEXA UTERI MASS ( 28 FDA reports)
BARRETT'S OESOPHAGUS ( 28 FDA reports)
CYSTITIS ( 28 FDA reports)
GOITRE ( 28 FDA reports)
HYDROCEPHALUS ( 28 FDA reports)
JOINT DISLOCATION ( 28 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 28 FDA reports)
MUSCLE STRAIN ( 28 FDA reports)
NASAL SEPTUM DEVIATION ( 28 FDA reports)
NEUTROPENIC SEPSIS ( 28 FDA reports)
ORAL CAVITY FISTULA ( 28 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 28 FDA reports)
SINUS CONGESTION ( 28 FDA reports)
SPLENIC LESION ( 28 FDA reports)
URINARY RETENTION ( 28 FDA reports)
ANOREXIA ( 27 FDA reports)
BIOPSY BONE MARROW ( 27 FDA reports)
DIALYSIS ( 27 FDA reports)
DIVERTICULITIS ( 27 FDA reports)
FLUSHING ( 27 FDA reports)
FOREIGN BODY ( 27 FDA reports)
HYPOACUSIS ( 27 FDA reports)
MACROGLOSSIA ( 27 FDA reports)
MASS EXCISION ( 27 FDA reports)
METASTASES TO LYMPH NODES ( 27 FDA reports)
OCULAR HYPERTENSION ( 27 FDA reports)
SENSORY LOSS ( 27 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 27 FDA reports)
ABDOMINAL PAIN LOWER ( 26 FDA reports)
ACUTE SINUSITIS ( 26 FDA reports)
BALANCE DISORDER ( 26 FDA reports)
BONE CYST ( 26 FDA reports)
BONE EROSION ( 26 FDA reports)
BREAST RECONSTRUCTION ( 26 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 26 FDA reports)
DERMATITIS ( 26 FDA reports)
FACE OEDEMA ( 26 FDA reports)
HYPERHIDROSIS ( 26 FDA reports)
HYPERKERATOSIS ( 26 FDA reports)
LIVER DISORDER ( 26 FDA reports)
MASTECTOMY ( 26 FDA reports)
MENISCUS LESION ( 26 FDA reports)
METAPLASIA ( 26 FDA reports)
MYOCARDITIS ( 26 FDA reports)
NASOPHARYNGITIS ( 26 FDA reports)
NEOPLASM ( 26 FDA reports)
NODULE ( 26 FDA reports)
OESOPHAGITIS ULCERATIVE ( 26 FDA reports)
OVERDOSE ( 26 FDA reports)
PROSTATOMEGALY ( 26 FDA reports)
PSEUDOMONAS INFECTION ( 26 FDA reports)
RHINITIS ALLERGIC ( 26 FDA reports)
SOFT TISSUE INFECTION ( 26 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 26 FDA reports)
THYROID NEOPLASM ( 26 FDA reports)
X-RAY ABNORMAL ( 26 FDA reports)
ACTINIC KERATOSIS ( 25 FDA reports)
BIOPSY BONE ABNORMAL ( 25 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 25 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 25 FDA reports)
DRUG HYPERSENSITIVITY ( 25 FDA reports)
DYSARTHRIA ( 25 FDA reports)
GRANULOCYTOPENIA ( 25 FDA reports)
HAEMODIALYSIS ( 25 FDA reports)
HYPOMAGNESAEMIA ( 25 FDA reports)
INFECTED SKIN ULCER ( 25 FDA reports)
MEMORY IMPAIRMENT ( 25 FDA reports)
NEURITIS ( 25 FDA reports)
NEUROPATHY ( 25 FDA reports)
PELVIC FRACTURE ( 25 FDA reports)
PETECHIAE ( 25 FDA reports)
PLASMACYTOMA ( 25 FDA reports)
SENSORY DISTURBANCE ( 25 FDA reports)
SKIN INDURATION ( 25 FDA reports)
ACCIDENT AT WORK ( 24 FDA reports)
B-CELL LYMPHOMA ( 24 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 24 FDA reports)
CULTURE URINE POSITIVE ( 24 FDA reports)
ECZEMA ( 24 FDA reports)
ENDOTRACHEAL INTUBATION ( 24 FDA reports)
GASTRIC ULCER ( 24 FDA reports)
GASTROENTERITIS ( 24 FDA reports)
GLAUCOMA ( 24 FDA reports)
HILAR LYMPHADENOPATHY ( 24 FDA reports)
HYPOCALCAEMIA ( 24 FDA reports)
JAUNDICE ( 24 FDA reports)
JOINT INJURY ( 24 FDA reports)
NEUROENDOCRINE CARCINOMA ( 24 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 24 FDA reports)
PHLEBITIS ( 24 FDA reports)
SKIN TIGHTNESS ( 24 FDA reports)
SPONDYLOLYSIS ( 24 FDA reports)
STRESS FRACTURE ( 24 FDA reports)
TINNITUS ( 24 FDA reports)
ADRENAL INSUFFICIENCY ( 23 FDA reports)
AGITATION ( 23 FDA reports)
ANGINA PECTORIS ( 23 FDA reports)
BLOOD UREA INCREASED ( 23 FDA reports)
CACHEXIA ( 23 FDA reports)
CLOSTRIDIUM COLITIS ( 23 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 23 FDA reports)
DRY EYE ( 23 FDA reports)
EPIGASTRIC DISCOMFORT ( 23 FDA reports)
HEART VALVE INCOMPETENCE ( 23 FDA reports)
HERPES SIMPLEX ( 23 FDA reports)
HYPOPHOSPHATAEMIA ( 23 FDA reports)
HYSTERECTOMY ( 23 FDA reports)
INTRAOCULAR LENS IMPLANT ( 23 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 23 FDA reports)
LIGAMENT RUPTURE ( 23 FDA reports)
LOCAL SWELLING ( 23 FDA reports)
LOCALISED INFECTION ( 23 FDA reports)
LUNG HYPERINFLATION ( 23 FDA reports)
MITRAL VALVE DISEASE ( 23 FDA reports)
MULTIPLE SCLEROSIS ( 23 FDA reports)
OEDEMA MUCOSAL ( 23 FDA reports)
ORAL HERPES ( 23 FDA reports)
OSTEOCHONDROSIS ( 23 FDA reports)
PANCREATITIS ( 23 FDA reports)
PARAPLEGIA ( 23 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 23 FDA reports)
PLEURODESIS ( 23 FDA reports)
POST PROCEDURAL COMPLICATION ( 23 FDA reports)
SUICIDAL IDEATION ( 23 FDA reports)
TONGUE DISCOLOURATION ( 23 FDA reports)
TUBERCULOSIS ( 23 FDA reports)
WOUND TREATMENT ( 23 FDA reports)
BODY TEMPERATURE INCREASED ( 22 FDA reports)
BREAST CANCER RECURRENT ( 22 FDA reports)
BRONCHOPNEUMONIA ( 22 FDA reports)
CARDIOVASCULAR DISORDER ( 22 FDA reports)
CATHETER REMOVAL ( 22 FDA reports)
CATHETERISATION CARDIAC ( 22 FDA reports)
CEREBRAL HAEMORRHAGE ( 22 FDA reports)
CHOLECYSTECTOMY ( 22 FDA reports)
DYSAESTHESIA ( 22 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 22 FDA reports)
FAECAL INCONTINENCE ( 22 FDA reports)
FANCONI SYNDROME ( 22 FDA reports)
FOOT FRACTURE ( 22 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 22 FDA reports)
INCREASED TENDENCY TO BRUISE ( 22 FDA reports)
ORAL SOFT TISSUE DISORDER ( 22 FDA reports)
OSTEORADIONECROSIS ( 22 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 22 FDA reports)
PSORIASIS ( 22 FDA reports)
PUBIS FRACTURE ( 22 FDA reports)
PURULENCE ( 22 FDA reports)
RASH MACULAR ( 22 FDA reports)
SKIN FIBROSIS ( 22 FDA reports)
SPINAL CORD COMPRESSION ( 22 FDA reports)
TUMOUR LYSIS SYNDROME ( 22 FDA reports)
URTICARIA ( 22 FDA reports)
AEROMONA INFECTION ( 21 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 21 FDA reports)
BACK DISORDER ( 21 FDA reports)
CATHETER PLACEMENT ( 21 FDA reports)
CORONARY ARTERY BYPASS ( 21 FDA reports)
DIASTOLIC DYSFUNCTION ( 21 FDA reports)
ENTEROCOCCAL INFECTION ( 21 FDA reports)
GINGIVAL ULCERATION ( 21 FDA reports)
LACTOSE INTOLERANCE ( 21 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 21 FDA reports)
MENOPAUSE ( 21 FDA reports)
MULTIPLE FRACTURES ( 21 FDA reports)
NEURODERMATITIS ( 21 FDA reports)
OESOPHAGEAL ULCER ( 21 FDA reports)
PARALYSIS ( 21 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 21 FDA reports)
SEXUAL DYSFUNCTION ( 21 FDA reports)
SKIN HYPERTROPHY ( 21 FDA reports)
STOMATOCYTES PRESENT ( 21 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 21 FDA reports)
URETHRAL CARUNCLE ( 21 FDA reports)
AXILLARY MASS ( 20 FDA reports)
BIOPSY LYMPH GLAND ( 20 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 20 FDA reports)
BRAIN OEDEMA ( 20 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 20 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 20 FDA reports)
FACET JOINT SYNDROME ( 20 FDA reports)
HAEMANGIOMA OF LIVER ( 20 FDA reports)
HEARING IMPAIRED ( 20 FDA reports)
HYPERTHYROIDISM ( 20 FDA reports)
JOINT CREPITATION ( 20 FDA reports)
MALIGNANT MELANOMA STAGE II ( 20 FDA reports)
METABOLIC ACIDOSIS ( 20 FDA reports)
MYOPIA ( 20 FDA reports)
PEPTIC ULCER ( 20 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 20 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 20 FDA reports)
RECTAL POLYP ( 20 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 20 FDA reports)
RETCHING ( 20 FDA reports)
SINUS BRADYCARDIA ( 20 FDA reports)
SQUAMOUS CELL CARCINOMA ( 20 FDA reports)
SUPERFICIAL SPREADING MELANOMA STAGE I ( 20 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 20 FDA reports)
SYNOVITIS ( 20 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 20 FDA reports)
WOUND DECOMPOSITION ( 20 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 19 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 19 FDA reports)
BREAST CYST ( 19 FDA reports)
CARDIAC VALVE DISEASE ( 19 FDA reports)
CERUMEN IMPACTION ( 19 FDA reports)
COLON CANCER ( 19 FDA reports)
CONJUNCTIVITIS VIRAL ( 19 FDA reports)
DELIRIUM ( 19 FDA reports)
DERMATITIS CONTACT ( 19 FDA reports)
DISEASE RECURRENCE ( 19 FDA reports)
DYSLIPIDAEMIA ( 19 FDA reports)
ESCHERICHIA BACTERAEMIA ( 19 FDA reports)
FACIAL PALSY ( 19 FDA reports)
FIBROMA ( 19 FDA reports)
IMMUNOSUPPRESSION ( 19 FDA reports)
INGROWING NAIL ( 19 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 19 FDA reports)
LACRIMATION INCREASED ( 19 FDA reports)
LIPOMA ( 19 FDA reports)
LUNG INFECTION ( 19 FDA reports)
MENINGITIS ( 19 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 19 FDA reports)
MYOCLONUS ( 19 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 19 FDA reports)
NEPHROPATHY ( 19 FDA reports)
NERVE BLOCK ( 19 FDA reports)
OBESITY ( 19 FDA reports)
ORAL DISCHARGE ( 19 FDA reports)
PLATELET COUNT INCREASED ( 19 FDA reports)
POLYNEUROPATHY ( 19 FDA reports)
RADICULAR PAIN ( 19 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 19 FDA reports)
SKIN NECROSIS ( 19 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 19 FDA reports)
TOOTH IMPACTED ( 19 FDA reports)
WOUND INFECTION ( 19 FDA reports)
APLASTIC ANAEMIA ( 18 FDA reports)
BONE TRIMMING ( 18 FDA reports)
BREAST CALCIFICATIONS ( 18 FDA reports)
BREAST CANCER FEMALE ( 18 FDA reports)
CAECITIS ( 18 FDA reports)
CIRCULATORY COLLAPSE ( 18 FDA reports)
CRANIAL NERVE DISORDER ( 18 FDA reports)
DYSPHONIA ( 18 FDA reports)
EMOTIONAL DISORDER ( 18 FDA reports)
EPICONDYLITIS ( 18 FDA reports)
GASTROINTESTINAL NECROSIS ( 18 FDA reports)
HEPATIC NEOPLASM ( 18 FDA reports)
HEPATITIS C ( 18 FDA reports)
INTESTINAL PERFORATION ( 18 FDA reports)
LIBIDO DECREASED ( 18 FDA reports)
LIMB DISCOMFORT ( 18 FDA reports)
METASTASES TO MENINGES ( 18 FDA reports)
MONOPARESIS ( 18 FDA reports)
MUCOSAL EROSION ( 18 FDA reports)
OEDEMA MOUTH ( 18 FDA reports)
OESOPHAGEAL PAIN ( 18 FDA reports)
OESOPHAGEAL STENOSIS ( 18 FDA reports)
OOPHORECTOMY ( 18 FDA reports)
PROSTHESIS IMPLANTATION ( 18 FDA reports)
RENAL TUBULAR NECROSIS ( 18 FDA reports)
SHOCK ( 18 FDA reports)
SKIN PLAQUE ( 18 FDA reports)
SPINAL FRACTURE ( 18 FDA reports)
T-CELL LYMPHOMA ( 18 FDA reports)
THORACOSTOMY ( 18 FDA reports)
VAGINAL DISCHARGE ( 18 FDA reports)
WOUND COMPLICATION ( 18 FDA reports)
ACUTE CORONARY SYNDROME ( 17 FDA reports)
AFFECTIVE DISORDER ( 17 FDA reports)
APPENDICECTOMY ( 17 FDA reports)
BIOPSY BREAST ABNORMAL ( 17 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 17 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 17 FDA reports)
BONE SCAN ABNORMAL ( 17 FDA reports)
BULLOUS LUNG DISEASE ( 17 FDA reports)
ECCHYMOSIS ( 17 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 17 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 17 FDA reports)
JOINT SPRAIN ( 17 FDA reports)
LIGAMENT SPRAIN ( 17 FDA reports)
MELAENA ( 17 FDA reports)
MORGANELLA INFECTION ( 17 FDA reports)
MYOSITIS ( 17 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 17 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 17 FDA reports)
ORAL INTAKE REDUCED ( 17 FDA reports)
OTORRHOEA ( 17 FDA reports)
PERIPHERAL COLDNESS ( 17 FDA reports)
RENAL ATROPHY ( 17 FDA reports)
RHINORRHOEA ( 17 FDA reports)
SPEECH DISORDER ( 17 FDA reports)
TONGUE PARALYSIS ( 17 FDA reports)
TOOTH RESORPTION ( 17 FDA reports)
VENOUS OCCLUSION ( 17 FDA reports)
ADDISON'S DISEASE ( 16 FDA reports)
AMENORRHOEA ( 16 FDA reports)
APPENDICITIS PERFORATED ( 16 FDA reports)
BLINDNESS ( 16 FDA reports)
BLOOD CALCIUM INCREASED ( 16 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 16 FDA reports)
BLOOD PRESSURE DECREASED ( 16 FDA reports)
BONE MARROW DEPRESSION ( 16 FDA reports)
BONE SARCOMA ( 16 FDA reports)
BRADYCARDIA ( 16 FDA reports)
BRAIN MASS ( 16 FDA reports)
BREAST PAIN ( 16 FDA reports)
COLONIC POLYP ( 16 FDA reports)
CSF PROTEIN INCREASED ( 16 FDA reports)
DEMENTIA ( 16 FDA reports)
DENTAL CARE ( 16 FDA reports)
DEPRESSED MOOD ( 16 FDA reports)
DUODENITIS ( 16 FDA reports)
EAR CONGESTION ( 16 FDA reports)
ERYTHEMA OF EYELID ( 16 FDA reports)
EXTREMITY NECROSIS ( 16 FDA reports)
FACIAL PARESIS ( 16 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 16 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 16 FDA reports)
GRAND MAL CONVULSION ( 16 FDA reports)
GYNAECOMASTIA ( 16 FDA reports)
HAIR GROWTH ABNORMAL ( 16 FDA reports)
HYPERPARATHYROIDISM ( 16 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 16 FDA reports)
KYPHOSCOLIOSIS ( 16 FDA reports)
MELANOCYTIC NAEVUS ( 16 FDA reports)
METABOLIC DISORDER ( 16 FDA reports)
NAIL DISORDER ( 16 FDA reports)
NECROSIS ( 16 FDA reports)
NERVOUSNESS ( 16 FDA reports)
OPTIC NEURITIS ( 16 FDA reports)
PALATAL DISORDER ( 16 FDA reports)
PARANASAL SINUS BENIGN NEOPLASM ( 16 FDA reports)
PARONYCHIA ( 16 FDA reports)
PROSTHESIS USER ( 16 FDA reports)
PULPITIS DENTAL ( 16 FDA reports)
RASH PAPULAR ( 16 FDA reports)
REFLUX OESOPHAGITIS ( 16 FDA reports)
SKIN BURNING SENSATION ( 16 FDA reports)
SPINAL FUSION SURGERY ( 16 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 16 FDA reports)
TOOTH EROSION ( 16 FDA reports)
TRACHEOSTOMY ( 16 FDA reports)
TUMOUR INVASION ( 16 FDA reports)
URINE OUTPUT DECREASED ( 16 FDA reports)
VENA CAVA THROMBOSIS ( 16 FDA reports)
VENTRICULAR HYPERTROPHY ( 16 FDA reports)
VERTEBRAL WEDGING ( 16 FDA reports)
WALKING AID USER ( 16 FDA reports)
APLASIA ( 15 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 15 FDA reports)
BACTERIAL TEST POSITIVE ( 15 FDA reports)
BENIGN OVARIAN TUMOUR ( 15 FDA reports)
BIOPSY BONE ( 15 FDA reports)
BLADDER NEOPLASM ( 15 FDA reports)
BLOOD POTASSIUM INCREASED ( 15 FDA reports)
BONE SWELLING ( 15 FDA reports)
CUBITAL TUNNEL SYNDROME ( 15 FDA reports)
CYSTOSCOPY ( 15 FDA reports)
DISTURBANCE IN ATTENTION ( 15 FDA reports)
DYSPHEMIA ( 15 FDA reports)
EROSIVE OESOPHAGITIS ( 15 FDA reports)
ESCHERICHIA SEPSIS ( 15 FDA reports)
FACIAL BONES FRACTURE ( 15 FDA reports)
FAECALOMA ( 15 FDA reports)
FAILURE TO THRIVE ( 15 FDA reports)
GANGRENE ( 15 FDA reports)
GOUT ( 15 FDA reports)
HEMIPARESIS ( 15 FDA reports)
HORDEOLUM ( 15 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 15 FDA reports)
IMPETIGO ( 15 FDA reports)
KIDNEY SMALL ( 15 FDA reports)
LUNG CONSOLIDATION ( 15 FDA reports)
NERVE ROOT COMPRESSION ( 15 FDA reports)
NEUROTOXICITY ( 15 FDA reports)
OCCULT BLOOD POSITIVE ( 15 FDA reports)
ONYCHALGIA ( 15 FDA reports)
OPEN WOUND ( 15 FDA reports)
OSTEOMA ( 15 FDA reports)
PANIC ATTACK ( 15 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 15 FDA reports)
PERFORMANCE STATUS DECREASED ( 15 FDA reports)
PNEUMONIA ASPIRATION ( 15 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 15 FDA reports)
RESTLESS LEGS SYNDROME ( 15 FDA reports)
RETINAL MELANOMA ( 15 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 15 FDA reports)
SINUS ARRHYTHMIA ( 15 FDA reports)
SKIN NEOPLASM EXCISION ( 15 FDA reports)
SPLENIC CYST ( 15 FDA reports)
TENDON INJURY ( 15 FDA reports)
THYROID CYST ( 15 FDA reports)
TRANSAMINASES INCREASED ( 15 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 15 FDA reports)
ABSCESS NECK ( 14 FDA reports)
ADRENAL MASS ( 14 FDA reports)
ALKALOSIS ( 14 FDA reports)
ANIMAL BITE ( 14 FDA reports)
ARTHROSCOPY ( 14 FDA reports)
ATRIAL FLUTTER ( 14 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 14 FDA reports)
BLADDER CYST ( 14 FDA reports)
BONE FISSURE ( 14 FDA reports)
BONE LOSS ( 14 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 14 FDA reports)
CAROTID BODY TUMOUR ( 14 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 14 FDA reports)
COLPOCELE ( 14 FDA reports)
CYST RUPTURE ( 14 FDA reports)
CYSTOCELE ( 14 FDA reports)
DERMOID CYST ( 14 FDA reports)
DEVICE RELATED SEPSIS ( 14 FDA reports)
DRY SKIN ( 14 FDA reports)
EYE SWELLING ( 14 FDA reports)
FEBRILE BONE MARROW APLASIA ( 14 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 14 FDA reports)
FISTULA DISCHARGE ( 14 FDA reports)
GENERALISED OEDEMA ( 14 FDA reports)
GRAFT VERSUS HOST DISEASE ( 14 FDA reports)
HAEMATOMA ( 14 FDA reports)
HYPERNATRAEMIA ( 14 FDA reports)
HYPOVOLAEMIA ( 14 FDA reports)
INFUSION RELATED REACTION ( 14 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 14 FDA reports)
MEDIASTINUM NEOPLASM ( 14 FDA reports)
METASTASES TO NASAL SINUSES ( 14 FDA reports)
MUSCLE INJURY ( 14 FDA reports)
MYOCARDIAL ISCHAEMIA ( 14 FDA reports)
NERVOUS SYSTEM DISORDER ( 14 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 14 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 14 FDA reports)
PAIN OF SKIN ( 14 FDA reports)
PANCREATIC CALCIFICATION ( 14 FDA reports)
PANCREATIC DISORDER ( 14 FDA reports)
PANCREATITIS ACUTE ( 14 FDA reports)
POLYP ( 14 FDA reports)
PROTEIN URINE ( 14 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 14 FDA reports)
PULMONARY ARTERY DILATATION ( 14 FDA reports)
RASH GENERALISED ( 14 FDA reports)
RECTOCELE ( 14 FDA reports)
RENAL MASS ( 14 FDA reports)
RESORPTION BONE INCREASED ( 14 FDA reports)
RIGHT ATRIAL DILATATION ( 14 FDA reports)
SENSATION OF FOREIGN BODY ( 14 FDA reports)
SICK SINUS SYNDROME ( 14 FDA reports)
SMEAR CERVIX ABNORMAL ( 14 FDA reports)
SPUTUM DISCOLOURED ( 14 FDA reports)
STOMATITIS NECROTISING ( 14 FDA reports)
STRESS URINARY INCONTINENCE ( 14 FDA reports)
SUPERINFECTION ( 14 FDA reports)
THROMBOPHLEBITIS ( 14 FDA reports)
TOOTH DEPOSIT ( 14 FDA reports)
VAGINAL PROLAPSE ( 14 FDA reports)
VENOUS INSUFFICIENCY ( 14 FDA reports)
VENTRICULAR HYPOKINESIA ( 14 FDA reports)
ABDOMINAL ABSCESS ( 13 FDA reports)
ADENOMA BENIGN ( 13 FDA reports)
ANGER ( 13 FDA reports)
APPENDICITIS ( 13 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 13 FDA reports)
BACTERIAL TEST NEGATIVE ( 13 FDA reports)
BLEPHARITIS ( 13 FDA reports)
BONE MARROW DISORDER ( 13 FDA reports)
BRONCHIECTASIS ( 13 FDA reports)
CALCIFIC DEPOSITS REMOVAL ( 13 FDA reports)
CALCULUS URETERIC ( 13 FDA reports)
CERVICOBRACHIAL SYNDROME ( 13 FDA reports)
CHOLECYSTITIS ( 13 FDA reports)
CLOSTRIDIAL INFECTION ( 13 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 13 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 13 FDA reports)
DRY MOUTH ( 13 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 13 FDA reports)
ERYTHEMA INFECTIOSUM ( 13 FDA reports)
GALLBLADDER POLYP ( 13 FDA reports)
GINGIVAL ATROPHY ( 13 FDA reports)
GOUTY ARTHRITIS ( 13 FDA reports)
HEPATIC CIRRHOSIS ( 13 FDA reports)
HEPATIC ENCEPHALOPATHY ( 13 FDA reports)
HYPERREFLEXIA ( 13 FDA reports)
HYPOAESTHESIA FACIAL ( 13 FDA reports)
HYPOALBUMINAEMIA ( 13 FDA reports)
INTERMITTENT CLAUDICATION ( 13 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 13 FDA reports)
LEFT ATRIAL DILATATION ( 13 FDA reports)
LENTIGO ( 13 FDA reports)
MECHANICAL VENTILATION ( 13 FDA reports)
MITRAL VALVE REPLACEMENT ( 13 FDA reports)
MUSCLE TIGHTNESS ( 13 FDA reports)
MUSCULOSKELETAL DISORDER ( 13 FDA reports)
NASAL POLYPS ( 13 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ( 13 FDA reports)
ORTHOPNOEA ( 13 FDA reports)
OXYGEN SUPPLEMENTATION ( 13 FDA reports)
PALLOR ( 13 FDA reports)
PANCREATIC ATROPHY ( 13 FDA reports)
PELVIC ADHESIONS ( 13 FDA reports)
POLYARTHRITIS ( 13 FDA reports)
POOR DENTAL CONDITION ( 13 FDA reports)
PRESYNCOPE ( 13 FDA reports)
PYELONEPHRITIS ( 13 FDA reports)
RADIATION OESOPHAGITIS ( 13 FDA reports)
RASH MACULO-PAPULAR ( 13 FDA reports)
RESPIRATORY DISORDER ( 13 FDA reports)
RETINAL INFARCTION ( 13 FDA reports)
SEBORRHOEIC KERATOSIS ( 13 FDA reports)
SINUS OPERATION ( 13 FDA reports)
TENOSYNOVITIS ( 13 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 13 FDA reports)
AGGRESSION ( 12 FDA reports)
APHASIA ( 12 FDA reports)
APICECTOMY ( 12 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 12 FDA reports)
ATRIOVENTRICULAR BLOCK ( 12 FDA reports)
ATROPHY ( 12 FDA reports)
BLOOD CULTURE POSITIVE ( 12 FDA reports)
BLOOD MAGNESIUM DECREASED ( 12 FDA reports)
BONE INFARCTION ( 12 FDA reports)
BONE NEOPLASM ( 12 FDA reports)
BREAST PROSTHESIS REMOVAL ( 12 FDA reports)
BURNS THIRD DEGREE ( 12 FDA reports)
CARBON DIOXIDE INCREASED ( 12 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 12 FDA reports)
CATHETER RELATED INFECTION ( 12 FDA reports)
CEREBRAL ISCHAEMIA ( 12 FDA reports)
CHOLESTEATOMA ( 12 FDA reports)
COLITIS ISCHAEMIC ( 12 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 12 FDA reports)
FACE INJURY ( 12 FDA reports)
FEMUR FRACTURE ( 12 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 12 FDA reports)
GLOMERULONEPHRITIS ( 12 FDA reports)
GLYCOSURIA ( 12 FDA reports)
HEPATITIS FULMINANT ( 12 FDA reports)
HEPATOMEGALY ( 12 FDA reports)
HYPERAESTHESIA ( 12 FDA reports)
HYPERSOMNIA ( 12 FDA reports)
INCISION SITE ERYTHEMA ( 12 FDA reports)
INCISION SITE OEDEMA ( 12 FDA reports)
IRRITABLE BOWEL SYNDROME ( 12 FDA reports)
JOINT SURGERY ( 12 FDA reports)
KERATITIS ( 12 FDA reports)
LHERMITTE'S SIGN ( 12 FDA reports)
MELANOSIS COLI ( 12 FDA reports)
MENTAL DISORDER ( 12 FDA reports)
MICTURITION URGENCY ( 12 FDA reports)
MOOD SWINGS ( 12 FDA reports)
MUSCLE DISORDER ( 12 FDA reports)
NEURODEGENERATIVE DISORDER ( 12 FDA reports)
OESOPHAGEAL SPASM ( 12 FDA reports)
OMENTUM NEOPLASM ( 12 FDA reports)
ORAL DYSAESTHESIA ( 12 FDA reports)
OXYGEN SATURATION DECREASED ( 12 FDA reports)
PANCOAST'S TUMOUR ( 12 FDA reports)
PAPILLOMA ( 12 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 12 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 12 FDA reports)
PHOTOSENSITIVITY REACTION ( 12 FDA reports)
PNEUMONIA BACTERIAL ( 12 FDA reports)
POLYDIPSIA ( 12 FDA reports)
PROTEIN TOTAL INCREASED ( 12 FDA reports)
PULMONARY MASS ( 12 FDA reports)
RED BLOOD CELLS URINE ( 12 FDA reports)
SACROILIITIS ( 12 FDA reports)
SKIN ATROPHY ( 12 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 12 FDA reports)
SPINAL COLUMN INJURY ( 12 FDA reports)
SPINAL X-RAY ABNORMAL ( 12 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 12 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 12 FDA reports)
TIC ( 12 FDA reports)
TOOTH DISCOLOURATION ( 12 FDA reports)
TRIGGER FINGER ( 12 FDA reports)
TYPE 2 DIABETES MELLITUS ( 12 FDA reports)
URINE ANALYSIS ( 12 FDA reports)
URINE ANALYSIS ABNORMAL ( 12 FDA reports)
VENTRICULAR DYSFUNCTION ( 12 FDA reports)
VERBAL ABUSE ( 12 FDA reports)
VIITH NERVE PARALYSIS ( 12 FDA reports)
VITAMIN D DEFICIENCY ( 12 FDA reports)
VULVOVAGINITIS ( 12 FDA reports)
WHITE BLOOD CELL COUNT ( 12 FDA reports)
ABASIA ( 11 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 11 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 11 FDA reports)
ADNEXA UTERI CYST ( 11 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 11 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 11 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 11 FDA reports)
BONE NEOPLASM MALIGNANT ( 11 FDA reports)
BREAST FIBROSIS ( 11 FDA reports)
BRONCHITIS CHRONIC ( 11 FDA reports)
CARDIAC OUTPUT DECREASED ( 11 FDA reports)
CERVICAL CORD COMPRESSION ( 11 FDA reports)
CERVICITIS HUMAN PAPILLOMA VIRUS ( 11 FDA reports)
CHEST WALL OPERATION ( 11 FDA reports)
CYST DRAINAGE ( 11 FDA reports)
CYTOLYTIC HEPATITIS ( 11 FDA reports)
DENTAL TREATMENT ( 11 FDA reports)
DIABETIC KETOACIDOSIS ( 11 FDA reports)
DRUG DEPENDENCE ( 11 FDA reports)
EMBOLISM VENOUS ( 11 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 11 FDA reports)
EXCORIATION ( 11 FDA reports)
GINGIVAL ABSCESS ( 11 FDA reports)
HYDROURETER ( 11 FDA reports)
INCISION SITE INFECTION ( 11 FDA reports)
LIGAMENT INJURY ( 11 FDA reports)
MENINGIOMA ( 11 FDA reports)
METASTASES TO HEART ( 11 FDA reports)
MITRAL VALVE CALCIFICATION ( 11 FDA reports)
NASAL DISORDER ( 11 FDA reports)
NECK MASS ( 11 FDA reports)
NEUROPATHIC ULCER ( 11 FDA reports)
ORTHOSIS USER ( 11 FDA reports)
OSTEOSARCOMA METASTATIC ( 11 FDA reports)
OTITIS MEDIA CHRONIC ( 11 FDA reports)
PERICARDITIS CONSTRICTIVE ( 11 FDA reports)
PERIOSTITIS ( 11 FDA reports)
PERONEAL NERVE PALSY ( 11 FDA reports)
PHARYNGEAL ERYTHEMA ( 11 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 11 FDA reports)
PROSTATISM ( 11 FDA reports)
PROTEIN TOTAL DECREASED ( 11 FDA reports)
PROTEIN URINE PRESENT ( 11 FDA reports)
PULMONARY HAEMORRHAGE ( 11 FDA reports)
SINUS POLYP ( 11 FDA reports)
TOOTH REPAIR ( 11 FDA reports)
TORTICOLLIS ( 11 FDA reports)
TUMOUR MARKER INCREASED ( 11 FDA reports)
UNRESPONSIVE TO STIMULI ( 11 FDA reports)
VASCULAR PSEUDOANEURYSM ( 11 FDA reports)
VERTEBRAL COLUMN MASS ( 11 FDA reports)
WOUND CLOSURE ( 11 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 10 FDA reports)
ABSCESS ORAL ( 10 FDA reports)
ACCIDENT ( 10 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 10 FDA reports)
ADRENAL SUPPRESSION ( 10 FDA reports)
AORTIC ANEURYSM ( 10 FDA reports)
APPETITE DISORDER ( 10 FDA reports)
ARTHRITIS BACTERIAL ( 10 FDA reports)
ASPERGILLOSIS ( 10 FDA reports)
ATAXIA ( 10 FDA reports)
BACTERIAL DIARRHOEA ( 10 FDA reports)
BLADDER PROLAPSE ( 10 FDA reports)
BLOOD BILIRUBIN INCREASED ( 10 FDA reports)
BREAST CANCER IN SITU ( 10 FDA reports)
CARDIAC FAILURE ACUTE ( 10 FDA reports)
CAROTID ARTERY STENOSIS ( 10 FDA reports)
CHARLES BONNET SYNDROME ( 10 FDA reports)
CHEST WALL MASS ( 10 FDA reports)
CYSTITIS HAEMORRHAGIC ( 10 FDA reports)
CYSTITIS KLEBSIELLA ( 10 FDA reports)
DERMAL CYST ( 10 FDA reports)
EAR NEOPLASM ( 10 FDA reports)
EYE DISCHARGE ( 10 FDA reports)
EYE DISORDER ( 10 FDA reports)
FACIAL NERVE DISORDER ( 10 FDA reports)
FOOD CRAVING ( 10 FDA reports)
GINGIVAL RECESSION ( 10 FDA reports)
GLOMERULOSCLEROSIS ( 10 FDA reports)
HAND DEFORMITY ( 10 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 10 FDA reports)
HYPOGLYCAEMIA ( 10 FDA reports)
IMMUNOGLOBULINS DECREASED ( 10 FDA reports)
INCONTINENCE ( 10 FDA reports)
INFECTIOUS PERITONITIS ( 10 FDA reports)
INFECTIVE TENOSYNOVITIS ( 10 FDA reports)
INTRACRANIAL ANEURYSM ( 10 FDA reports)
KIDNEY INFECTION ( 10 FDA reports)
LABORATORY TEST ABNORMAL ( 10 FDA reports)
LEUKAEMIA ( 10 FDA reports)
MACULOPATHY ( 10 FDA reports)
MAJOR DEPRESSION ( 10 FDA reports)
MENSTRUAL DISORDER ( 10 FDA reports)
METASTASES TO PERITONEUM ( 10 FDA reports)
METASTASES TO THE MEDIASTINUM ( 10 FDA reports)
NO THERAPEUTIC RESPONSE ( 10 FDA reports)
OLIGURIA ( 10 FDA reports)
OPEN REDUCTION OF FRACTURE ( 10 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 10 FDA reports)
OROANTRAL FISTULA ( 10 FDA reports)
OVARIAN FAILURE ( 10 FDA reports)
PARAPARESIS ( 10 FDA reports)
PATELLA FRACTURE ( 10 FDA reports)
PELVIC HAEMATOMA ( 10 FDA reports)
PERIARTHRITIS ( 10 FDA reports)
PERICARDITIS ( 10 FDA reports)
PILONIDAL CYST ( 10 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 10 FDA reports)
POOR PERIPHERAL CIRCULATION ( 10 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 10 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 10 FDA reports)
RADIATION PNEUMONITIS ( 10 FDA reports)
RADIATION SKIN INJURY ( 10 FDA reports)
RADIUS FRACTURE ( 10 FDA reports)
RASH MORBILLIFORM ( 10 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 10 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 10 FDA reports)
SENSATION OF HEAVINESS ( 10 FDA reports)
STREPTOCOCCAL INFECTION ( 10 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 10 FDA reports)
SYNOVIAL RUPTURE ( 10 FDA reports)
THYROID DISORDER ( 10 FDA reports)
THYROIDITIS ( 10 FDA reports)
UROSEPSIS ( 10 FDA reports)
VASCULAR CALCIFICATION ( 10 FDA reports)
VENOUS THROMBOSIS ( 10 FDA reports)
VISUAL ACUITY REDUCED ( 10 FDA reports)
VITREOUS FLOATERS ( 10 FDA reports)
VULVOVAGINAL DRYNESS ( 10 FDA reports)
WOUND ( 10 FDA reports)
ACUTE HEPATIC FAILURE ( 9 FDA reports)
ADRENAL ADENOMA ( 9 FDA reports)
ANAL ULCER ( 9 FDA reports)
ANGIOPLASTY ( 9 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 9 FDA reports)
ASPHYXIA ( 9 FDA reports)
BIPOLAR DISORDER ( 9 FDA reports)
BLADDER NECK OPERATION ( 9 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 9 FDA reports)
BRACHIAL PLEXOPATHY ( 9 FDA reports)
BREAST DISCHARGE ( 9 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 9 FDA reports)
CARDIAC OPERATION ( 9 FDA reports)
CATHETER RELATED COMPLICATION ( 9 FDA reports)
CATHETER SEPSIS ( 9 FDA reports)
CERVICITIS ( 9 FDA reports)
COMPUTERISED TOMOGRAM ( 9 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 9 FDA reports)
CORNEAL OPERATION ( 9 FDA reports)
CYSTOPEXY ( 9 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 9 FDA reports)
EOSINOPHILIA ( 9 FDA reports)
EXTRAVASATION ( 9 FDA reports)
FIBROADENOMA OF BREAST ( 9 FDA reports)
GASTRODUODENITIS ( 9 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 9 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 9 FDA reports)
HEPATIC ENZYME ABNORMAL ( 9 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 9 FDA reports)
HERNIA ( 9 FDA reports)
HUMERUS FRACTURE ( 9 FDA reports)
HYPERCAPNIA ( 9 FDA reports)
HYPOKINESIA ( 9 FDA reports)
INJECTION SITE PAIN ( 9 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 9 FDA reports)
MALLORY-WEISS SYNDROME ( 9 FDA reports)
MASTOIDITIS ( 9 FDA reports)
METASTASES TO KIDNEY ( 9 FDA reports)
METASTASES TO SPLEEN ( 9 FDA reports)
MONARTHRITIS ( 9 FDA reports)
MONOCYTE COUNT INCREASED ( 9 FDA reports)
MYOPATHY ( 9 FDA reports)
OESOPHAGEAL POLYP ( 9 FDA reports)
PERIODONTAL INFECTION ( 9 FDA reports)
PERTUSSIS ( 9 FDA reports)
PHAEOCHROMOCYTOMA ( 9 FDA reports)
PREMATURE BABY ( 9 FDA reports)
PSYCHOTIC DISORDER ( 9 FDA reports)
PYELOCALIECTASIS ( 9 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 9 FDA reports)
RENAL CANCER ( 9 FDA reports)
RESPIRATORY ARREST ( 9 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 9 FDA reports)
SCAPULA FRACTURE ( 9 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 9 FDA reports)
SKIN LACERATION ( 9 FDA reports)
SPINAL LAMINECTOMY ( 9 FDA reports)
STRESS ( 9 FDA reports)
THROMBECTOMY ( 9 FDA reports)
TREATMENT NONCOMPLIANCE ( 9 FDA reports)
TRISMUS ( 9 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 9 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 9 FDA reports)
URETERIC OBSTRUCTION ( 9 FDA reports)
VARICELLA ( 9 FDA reports)
VENTRICULO-PERITONEAL SHUNT ( 9 FDA reports)
ACANTHOSIS NIGRICANS ( 8 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 8 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 8 FDA reports)
ADENOCARCINOMA ( 8 FDA reports)
ADENOVIRUS INFECTION ( 8 FDA reports)
ADRENAL NEOPLASM ( 8 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 8 FDA reports)
AMYLOIDOSIS ( 8 FDA reports)
AORTIC VALVE DISEASE ( 8 FDA reports)
APNOEA ( 8 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 8 FDA reports)
BLINDNESS TRANSIENT ( 8 FDA reports)
BLOOD DISORDER ( 8 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 8 FDA reports)
BONE FISTULA ( 8 FDA reports)
BREAST DISORDER ( 8 FDA reports)
BREAST NECROSIS ( 8 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 8 FDA reports)
BRONCHOSPASM ( 8 FDA reports)
CARDIOGENIC SHOCK ( 8 FDA reports)
COLONOSCOPY ABNORMAL ( 8 FDA reports)
COORDINATION ABNORMAL ( 8 FDA reports)
CRYING ( 8 FDA reports)
CYANOSIS ( 8 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 8 FDA reports)
DRUG ABUSE ( 8 FDA reports)
EAR HAEMORRHAGE ( 8 FDA reports)
ECZEMA EYELIDS ( 8 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 8 FDA reports)
ENCEPHALITIS ( 8 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 8 FDA reports)
EROSIVE DUODENITIS ( 8 FDA reports)
ESSENTIAL HYPERTENSION ( 8 FDA reports)
EXTRASYSTOLES ( 8 FDA reports)
FAECES DISCOLOURED ( 8 FDA reports)
FISTULA REPAIR ( 8 FDA reports)
FOREIGN BODY TRAUMA ( 8 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 8 FDA reports)
HEAD INJURY ( 8 FDA reports)
HEPATOSPLENOMEGALY ( 8 FDA reports)
HIDRADENITIS ( 8 FDA reports)
HYPERALBUMINAEMIA ( 8 FDA reports)
INTESTINAL OBSTRUCTION ( 8 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 8 FDA reports)
LEIOMYOSARCOMA METASTATIC ( 8 FDA reports)
LIMB INJURY ( 8 FDA reports)
LOBAR PNEUMONIA ( 8 FDA reports)
LUNG CANCER METASTATIC ( 8 FDA reports)
MACROCYTOSIS ( 8 FDA reports)
MAMMOPLASTY ( 8 FDA reports)
MEDICATION ERROR ( 8 FDA reports)
MENISCUS REMOVAL ( 8 FDA reports)
MENTAL IMPAIRMENT ( 8 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 8 FDA reports)
METASTASES TO MUSCLE ( 8 FDA reports)
NEOPLASM SKIN ( 8 FDA reports)
NEUROGENIC BLADDER ( 8 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 8 FDA reports)
OPEN FRACTURE ( 8 FDA reports)
OSTEOSYNTHESIS ( 8 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 8 FDA reports)
PAROTID GLAND ENLARGEMENT ( 8 FDA reports)
PAROTITIS ( 8 FDA reports)
PHOTOPHOBIA ( 8 FDA reports)
PITTING OEDEMA ( 8 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 8 FDA reports)
PLATELET TRANSFUSION ( 8 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 8 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 8 FDA reports)
PULMONARY HILUM MASS ( 8 FDA reports)
QUALITY OF LIFE DECREASED ( 8 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
RIB DEFORMITY ( 8 FDA reports)
SINUS HEADACHE ( 8 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 8 FDA reports)
STRESS ULCER ( 8 FDA reports)
SUBCUTANEOUS NODULE ( 8 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 8 FDA reports)
TENDON DISORDER ( 8 FDA reports)
THERMAL BURN ( 8 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 8 FDA reports)
TOE WALKING ( 8 FDA reports)
UMBILICAL HERNIA ( 8 FDA reports)
VARICES OESOPHAGEAL ( 8 FDA reports)
VENTRICULAR FIBRILLATION ( 8 FDA reports)
VENTRICULAR TACHYCARDIA ( 8 FDA reports)
VIRAL PHARYNGITIS ( 8 FDA reports)
ACUTE RESPIRATORY FAILURE ( 7 FDA reports)
ADRENAL DISORDER ( 7 FDA reports)
ANAPHYLACTIC REACTION ( 7 FDA reports)
AORTIC VALVE CALCIFICATION ( 7 FDA reports)
AORTIC VALVE STENOSIS ( 7 FDA reports)
APICAL GRANULOMA ( 7 FDA reports)
APLASIA PURE RED CELL ( 7 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 7 FDA reports)
BILIARY COLIC ( 7 FDA reports)
BILIARY DYSKINESIA ( 7 FDA reports)
BLADDER DYSFUNCTION ( 7 FDA reports)
BLISTER ( 7 FDA reports)
BLOOD COUNT ABNORMAL ( 7 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 7 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 7 FDA reports)
CELLULITIS STREPTOCOCCAL ( 7 FDA reports)
CENTRAL LINE INFECTION ( 7 FDA reports)
CHLOASMA ( 7 FDA reports)
CHONDROMALACIA ( 7 FDA reports)
CHONDROPATHY ( 7 FDA reports)
CHRONIC GRANULOMATOUS DISEASE ( 7 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 7 FDA reports)
COLECTOMY ( 7 FDA reports)
COLONIC STENOSIS ( 7 FDA reports)
DEVICE OCCLUSION ( 7 FDA reports)
DIABETIC NEUROPATHY ( 7 FDA reports)
DRUG INTOLERANCE ( 7 FDA reports)
DUODENAL STENOSIS ( 7 FDA reports)
DUODENAL ULCER ( 7 FDA reports)
EAR DISORDER ( 7 FDA reports)
EFFUSION ( 7 FDA reports)
EOSINOPHIL COUNT INCREASED ( 7 FDA reports)
ERYTHEMA NODOSUM ( 7 FDA reports)
FEBRILE INFECTION ( 7 FDA reports)
GALLBLADDER CANCER ( 7 FDA reports)
GASTRIC CANCER ( 7 FDA reports)
GASTROENTERITIS VIRAL ( 7 FDA reports)
GINGIVAL HYPERTROPHY ( 7 FDA reports)
HALLUCINATION, AUDITORY ( 7 FDA reports)
HEPATIC ENZYME INCREASED ( 7 FDA reports)
HEPATITIS ACUTE ( 7 FDA reports)
HERPES ZOSTER DISSEMINATED ( 7 FDA reports)
HYPERBILIRUBINAEMIA ( 7 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 7 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 7 FDA reports)
INCISIONAL DRAINAGE ( 7 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 7 FDA reports)
LARYNGITIS ( 7 FDA reports)
LIMB OPERATION ( 7 FDA reports)
LIPODYSTROPHY ACQUIRED ( 7 FDA reports)
MARROW HYPERPLASIA ( 7 FDA reports)
MENORRHAGIA ( 7 FDA reports)
METASTASES TO BONE MARROW ( 7 FDA reports)
METASTASES TO PANCREAS ( 7 FDA reports)
METASTASES TO PLEURA ( 7 FDA reports)
MITRAL VALVE STENOSIS ( 7 FDA reports)
MUCOSAL NECROSIS ( 7 FDA reports)
MUCOUS MEMBRANE DISORDER ( 7 FDA reports)
MUSCLE ATROPHY ( 7 FDA reports)
NASOPHARYNGEAL CANCER ( 7 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 7 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 7 FDA reports)
ONYCHOCLASIS ( 7 FDA reports)
OOPHORECTOMY BILATERAL ( 7 FDA reports)
OPTIC NEUROPATHY ( 7 FDA reports)
PANCREATIC NEOPLASM ( 7 FDA reports)
PERCUSSION TEST ABNORMAL ( 7 FDA reports)
PERITONITIS ( 7 FDA reports)
PHARYNGEAL OEDEMA ( 7 FDA reports)
PHOSPHORUS METABOLISM DISORDER ( 7 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 7 FDA reports)
POST PROCEDURAL DISCHARGE ( 7 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 7 FDA reports)
PRESBYOPIA ( 7 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA STAGE II ( 7 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 7 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 7 FDA reports)
RENAL CELL CARCINOMA ( 7 FDA reports)
RENAL TUBULAR DISORDER ( 7 FDA reports)
RESUSCITATION ( 7 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 7 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 7 FDA reports)
ROSACEA ( 7 FDA reports)
SINUS RHYTHM ( 7 FDA reports)
SKIN LESION EXCISION ( 7 FDA reports)
SKIN REACTION ( 7 FDA reports)
SPINAL CORPECTOMY ( 7 FDA reports)
SUDDEN DEATH ( 7 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 7 FDA reports)
TENDON SHEATH INCISION ( 7 FDA reports)
THERAPY NON-RESPONDER ( 7 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 7 FDA reports)
THYMUS DISORDER ( 7 FDA reports)
THYROID HORMONE REPLACEMENT THERAPY ( 7 FDA reports)
URETHRAL STENOSIS ( 7 FDA reports)
ANAPHYLACTIC SHOCK ( 6 FDA reports)
ANGIOPATHY ( 6 FDA reports)
ANOSMIA ( 6 FDA reports)
APHTHOUS STOMATITIS ( 6 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 6 FDA reports)
ASTIGMATISM ( 6 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 6 FDA reports)
BLADDER CANCER ( 6 FDA reports)
BLOOD AMYLASE INCREASED ( 6 FDA reports)
BLOOD GLUCOSE DECREASED ( 6 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 6 FDA reports)
BONE GRAFT ( 6 FDA reports)
BONE MARROW NECROSIS ( 6 FDA reports)
BREAST ENLARGEMENT ( 6 FDA reports)
BREAST HYPERPLASIA ( 6 FDA reports)
BRONCHOPLEURAL FISTULA ( 6 FDA reports)
BURNING SENSATION ( 6 FDA reports)
CARDIAC PACEMAKER INSERTION ( 6 FDA reports)
CAROTID ARTERY DISEASE ( 6 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 6 FDA reports)
CERVIX CARCINOMA ( 6 FDA reports)
CLAUSTROPHOBIA ( 6 FDA reports)
COGNITIVE DISORDER ( 6 FDA reports)
COLITIS ULCERATIVE ( 6 FDA reports)
COLLATERAL CIRCULATION ( 6 FDA reports)
CREPITATIONS ( 6 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 6 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 6 FDA reports)
DRUG EFFECT DECREASED ( 6 FDA reports)
DRUG ERUPTION ( 6 FDA reports)
DUODENAL POLYP ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 6 FDA reports)
ENDARTERECTOMY ( 6 FDA reports)
ENTERITIS ( 6 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 6 FDA reports)
ENTEROCOLITIS ( 6 FDA reports)
EPHELIDES ( 6 FDA reports)
FOOD POISONING ( 6 FDA reports)
FOOT DEFORMITY ( 6 FDA reports)
FRACTURE NONUNION ( 6 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 6 FDA reports)
HAEMATEMESIS ( 6 FDA reports)
HAEMOLYTIC ANAEMIA ( 6 FDA reports)
HAEMORRHAGE URINARY TRACT ( 6 FDA reports)
HALLUCINATION ( 6 FDA reports)
HEART RATE DECREASED ( 6 FDA reports)
HEPATITIS CHOLESTATIC ( 6 FDA reports)
HODGKIN'S DISEASE RECURRENT ( 6 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 6 FDA reports)
HYDROPNEUMOTHORAX ( 6 FDA reports)
HYPERPHOSPHATAEMIA ( 6 FDA reports)
HYPERTONIC BLADDER ( 6 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 6 FDA reports)
JOINT ARTHROPLASTY ( 6 FDA reports)
KELOID SCAR ( 6 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 6 FDA reports)
KNEE ARTHROPLASTY ( 6 FDA reports)
LOWER EXTREMITY MASS ( 6 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 6 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 6 FDA reports)
MALIGNANT TUMOUR EXCISION ( 6 FDA reports)
MANDIBULECTOMY ( 6 FDA reports)
MEDIASTINAL BIOPSY ( 6 FDA reports)
MEDIASTINAL MASS ( 6 FDA reports)
MEDICAL DEVICE REMOVAL ( 6 FDA reports)
METASTASES TO ADRENALS ( 6 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 6 FDA reports)
MONONEURITIS ( 6 FDA reports)
MYELOID LEUKAEMIA ( 6 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 6 FDA reports)
NAIL DISCOLOURATION ( 6 FDA reports)
NASAL DISCOMFORT ( 6 FDA reports)
NASAL ULCER ( 6 FDA reports)
OBSTRUCTION ( 6 FDA reports)
ONYCHOGRYPHOSIS ( 6 FDA reports)
ONYCHOMADESIS ( 6 FDA reports)
PARALYSIS FLACCID ( 6 FDA reports)
PARTNER STRESS ( 6 FDA reports)
PEAU D'ORANGE ( 6 FDA reports)
PERICARDIAL DISEASE ( 6 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 6 FDA reports)
PNEUMONIA FUNGAL ( 6 FDA reports)
PNEUMONIA VIRAL ( 6 FDA reports)
POLYURIA ( 6 FDA reports)
POST-TRAUMATIC OSTEOPOROSIS ( 6 FDA reports)
PROCTALGIA ( 6 FDA reports)
PROSTATE CANCER ( 6 FDA reports)
PROSTATITIS ( 6 FDA reports)
PULMONARY AIR LEAKAGE ( 6 FDA reports)
RADIATION INJURY ( 6 FDA reports)
RECTAL CANCER ( 6 FDA reports)
RESIDUAL URINE VOLUME ( 6 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 6 FDA reports)
SACRALISATION ( 6 FDA reports)
SEASONAL ALLERGY ( 6 FDA reports)
SKIN FISSURES ( 6 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 6 FDA reports)
SUBDURAL HAEMATOMA ( 6 FDA reports)
TENDON GRAFT ( 6 FDA reports)
TESTICULAR MASS ( 6 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 6 FDA reports)
THYROID CANCER ( 6 FDA reports)
TOBACCO ABUSE ( 6 FDA reports)
URETHRITIS ( 6 FDA reports)
VASCULITIS ( 6 FDA reports)
VERTEBROPLASTY ( 6 FDA reports)
VISUAL FIELD DEFECT ( 6 FDA reports)
VITAMIN B12 DEFICIENCY ( 6 FDA reports)
VOCAL CORD PARALYSIS ( 6 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 6 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 6 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 6 FDA reports)
ACETABULUM FRACTURE ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 5 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 5 FDA reports)
ANEURYSM ( 5 FDA reports)
AORTIC BRUIT ( 5 FDA reports)
AORTIC VALVE SCLEROSIS ( 5 FDA reports)
ARTERIOVENOUS MALFORMATION ( 5 FDA reports)
ASPIRATION ( 5 FDA reports)
AURICULAR PERICHONDRITIS ( 5 FDA reports)
AUTISM SPECTRUM DISORDER ( 5 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 5 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 5 FDA reports)
BLOOD CHLORIDE DECREASED ( 5 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 5 FDA reports)
BLOOD UREA DECREASED ( 5 FDA reports)
BRAIN CANCER METASTATIC ( 5 FDA reports)
BREAST HAEMATOMA ( 5 FDA reports)
CARDIAC TAMPONADE ( 5 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 5 FDA reports)
CATHETER SITE ERYTHEMA ( 5 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 5 FDA reports)
CEREBRAL HAEMATOMA ( 5 FDA reports)
CEREBROSPINAL FLUID RESERVOIR PLACEMENT ( 5 FDA reports)
CHOLECYSTITIS ACUTE ( 5 FDA reports)
CHROMOSOME ABNORMALITY ( 5 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 5 FDA reports)
COLON POLYPECTOMY ( 5 FDA reports)
CUSHINGOID ( 5 FDA reports)
DECREASED ACTIVITY ( 5 FDA reports)
DIABETIC FOOT ( 5 FDA reports)
DRUG RESISTANCE ( 5 FDA reports)
DRUG TOLERANCE DECREASED ( 5 FDA reports)
DYSTONIA ( 5 FDA reports)
EARLY SATIETY ( 5 FDA reports)
EATING DISORDER SYMPTOM ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 5 FDA reports)
ENDOMETRIAL ATROPHY ( 5 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 5 FDA reports)
ENGRAFTMENT SYNDROME ( 5 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 5 FDA reports)
FASCIITIS ( 5 FDA reports)
FOETAL GROWTH RESTRICTION ( 5 FDA reports)
FULL BLOOD COUNT DECREASED ( 5 FDA reports)
GASTRITIS EROSIVE ( 5 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 5 FDA reports)
HAEMATOTOXICITY ( 5 FDA reports)
HAEMORRHAGIC STROKE ( 5 FDA reports)
HEPATIC HAEMORRHAGE ( 5 FDA reports)
HERNIA REPAIR ( 5 FDA reports)
HOSPICE CARE ( 5 FDA reports)
HYDROCELE ( 5 FDA reports)
HYDROMYELIA ( 5 FDA reports)
HYPOPNOEA ( 5 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 5 FDA reports)
IMPULSE-CONTROL DISORDER ( 5 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 5 FDA reports)
INTESTINAL POLYP ( 5 FDA reports)
INTESTINAL STENOSIS ( 5 FDA reports)
JOINT CONTRACTURE ( 5 FDA reports)
KETONURIA ( 5 FDA reports)
LABILE BLOOD PRESSURE ( 5 FDA reports)
LEUKAEMIA PLASMACYTIC ( 5 FDA reports)
LICHENOID KERATOSIS ( 5 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 5 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 5 FDA reports)
MOOD ALTERED ( 5 FDA reports)
MULTIPLE INJURIES ( 5 FDA reports)
MYOCARDIAL FIBROSIS ( 5 FDA reports)
NEPHROGENIC ANAEMIA ( 5 FDA reports)
NERVE INJURY ( 5 FDA reports)
NEUTROPENIC INFECTION ( 5 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 5 FDA reports)
NICOTINE DEPENDENCE ( 5 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 5 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 5 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 5 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 5 FDA reports)
OVARIAN ADHESION ( 5 FDA reports)
OVERWEIGHT ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
PHOTOPSIA ( 5 FDA reports)
PLEURISY ( 5 FDA reports)
POSTMENOPAUSE ( 5 FDA reports)
PULMONARY VASCULAR DISORDER ( 5 FDA reports)
PYOGENIC GRANULOMA ( 5 FDA reports)
QRS AXIS ABNORMAL ( 5 FDA reports)
RADICAL MASTECTOMY ( 5 FDA reports)
RESPIRATORY RATE INCREASED ( 5 FDA reports)
RETICULOCYTE COUNT INCREASED ( 5 FDA reports)
RHINITIS SEASONAL ( 5 FDA reports)
SALIVARY GLAND MASS ( 5 FDA reports)
SARCOMA OF SKIN ( 5 FDA reports)
SINUSITIS FUNGAL ( 5 FDA reports)
SKIN HYPOPIGMENTATION ( 5 FDA reports)
SKIN NODULE ( 5 FDA reports)
SNORING ( 5 FDA reports)
SPLENIC ARTERY ANEURYSM ( 5 FDA reports)
SPLINT APPLICATION ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
SWOLLEN TONGUE ( 5 FDA reports)
TACHYARRHYTHMIA ( 5 FDA reports)
TACHYPNOEA ( 5 FDA reports)
THROAT TIGHTNESS ( 5 FDA reports)
THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
TOXIC SKIN ERUPTION ( 5 FDA reports)
TROPONIN I INCREASED ( 5 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 5 FDA reports)
URETERIC DILATATION ( 5 FDA reports)
UTERINE ATONY ( 5 FDA reports)
UTERINE PROLAPSE ( 5 FDA reports)
VARICOSE VEIN ( 5 FDA reports)
VENA CAVA FILTER INSERTION ( 5 FDA reports)
VOCAL CORD POLYP ( 5 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 5 FDA reports)
WEIGHT BEARING DIFFICULTY ( 5 FDA reports)
WEIGHT FLUCTUATION ( 5 FDA reports)
XEROSIS ( 5 FDA reports)
ABDOMINAL MASS ( 4 FDA reports)
ABDOMINAL SYMPTOM ( 4 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 4 FDA reports)
ACUTE PSYCHOSIS ( 4 FDA reports)
ADVERSE EVENT ( 4 FDA reports)
ALVEOLITIS ALLERGIC ( 4 FDA reports)
ARTERIAL STENOSIS ( 4 FDA reports)
BILE DUCT CANCER ( 4 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 4 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 4 FDA reports)
BLOOD URIC ACID INCREASED ( 4 FDA reports)
BONE CANCER METASTATIC ( 4 FDA reports)
BONE MARROW TOXICITY ( 4 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 4 FDA reports)
BREAST LUMP REMOVAL ( 4 FDA reports)
BREAST OPERATION ( 4 FDA reports)
BRONCHIAL DISORDER ( 4 FDA reports)
CATARACT NUCLEAR ( 4 FDA reports)
CAUDA EQUINA SYNDROME ( 4 FDA reports)
CEREBELLAR ATAXIA ( 4 FDA reports)
CEREBELLAR ATROPHY ( 4 FDA reports)
CHEMOTHERAPY ( 4 FDA reports)
CHEST TUBE INSERTION ( 4 FDA reports)
CHEST X-RAY ABNORMAL ( 4 FDA reports)
COR PULMONALE ( 4 FDA reports)
CORNEAL EROSION ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 4 FDA reports)
CUTIS LAXA ( 4 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 4 FDA reports)
DENERVATION ATROPHY ( 4 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 4 FDA reports)
DIVERTICULAR PERFORATION ( 4 FDA reports)
DRUG LEVEL INCREASED ( 4 FDA reports)
DUODENAL PERFORATION ( 4 FDA reports)
EMBOLIC STROKE ( 4 FDA reports)
ENTHESOPATHY ( 4 FDA reports)
EPIDERMAL NECROSIS ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
EXPLORATIVE LAPAROTOMY ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
EYELID PTOSIS ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
FEMORAL ARTERY OCCLUSION ( 4 FDA reports)
FURUNCLE ( 4 FDA reports)
GASTROENTERITIS BACTERIAL ( 4 FDA reports)
GASTROINTESTINAL PERFORATION ( 4 FDA reports)
GASTROSTOMY TUBE INSERTION ( 4 FDA reports)
GINGIVAL OPERATION ( 4 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 4 FDA reports)
GUILLAIN-BARRE SYNDROME ( 4 FDA reports)
HIP SURGERY ( 4 FDA reports)
ILL-DEFINED DISORDER ( 4 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 4 FDA reports)
INGUINAL MASS ( 4 FDA reports)
INJECTION SITE ERYTHEMA ( 4 FDA reports)
INTESTINAL DILATATION ( 4 FDA reports)
INTUBATION ( 4 FDA reports)
JOINT DESTRUCTION ( 4 FDA reports)
KNEE OPERATION ( 4 FDA reports)
LATEX ALLERGY ( 4 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 4 FDA reports)
LIP ULCERATION ( 4 FDA reports)
LIPOATROPHY ( 4 FDA reports)
LYMPH NODE PAIN ( 4 FDA reports)
LYMPHOPENIA ( 4 FDA reports)
MACULAR DEGENERATION ( 4 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 4 FDA reports)
MASTOID DISORDER ( 4 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 4 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 4 FDA reports)
METABOLIC ENCEPHALOPATHY ( 4 FDA reports)
METABOLIC SYNDROME ( 4 FDA reports)
METASTASES TO OVARY ( 4 FDA reports)
MICROVASCULAR ANGINA ( 4 FDA reports)
MIOSIS ( 4 FDA reports)
MIXED HYPERLIPIDAEMIA ( 4 FDA reports)
MONOCYTE COUNT DECREASED ( 4 FDA reports)
NEOPLASM RECURRENCE ( 4 FDA reports)
NEPHROTIC SYNDROME ( 4 FDA reports)
OBSTRUCTIVE UROPATHY ( 4 FDA reports)
OCULAR HYPERAEMIA ( 4 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 4 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 4 FDA reports)
ORCHITIS ( 4 FDA reports)
ORGAN FAILURE ( 4 FDA reports)
OVARIAN ATROPHY ( 4 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 4 FDA reports)
PARANOIA ( 4 FDA reports)
PCO2 DECREASED ( 4 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 4 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 4 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 4 FDA reports)
PRODUCT QUALITY ISSUE ( 4 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 4 FDA reports)
PULMONARY CALCIFICATION ( 4 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 4 FDA reports)
PULMONARY GRANULOMA ( 4 FDA reports)
PULMONARY INFARCTION ( 4 FDA reports)
PULMONARY MYCOSIS ( 4 FDA reports)
PULMONARY THROMBOSIS ( 4 FDA reports)
RADICULITIS ( 4 FDA reports)
RALES ( 4 FDA reports)
RASH VESICULAR ( 4 FDA reports)
RECURRENT CANCER ( 4 FDA reports)
RESPIRATION ABNORMAL ( 4 FDA reports)
RESPIRATORY ACIDOSIS ( 4 FDA reports)
RETINAL HAEMORRHAGE ( 4 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 4 FDA reports)
SEBORRHOEIC DERMATITIS ( 4 FDA reports)
SERRATIA SEPSIS ( 4 FDA reports)
SERUM FERRITIN INCREASED ( 4 FDA reports)
SIALOADENITIS ( 4 FDA reports)
SKIN HAEMORRHAGE ( 4 FDA reports)
SPONDYLITIS ( 4 FDA reports)
STRONGYLOIDIASIS ( 4 FDA reports)
SUBACUTE ENDOCARDITIS ( 4 FDA reports)
SUBMANDIBULAR MASS ( 4 FDA reports)
SUFFOCATION FEELING ( 4 FDA reports)
SYNCOPE VASOVAGAL ( 4 FDA reports)
SYSTEMIC CANDIDA ( 4 FDA reports)
TENDON RUPTURE ( 4 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 4 FDA reports)
THROMBOCYTOSIS ( 4 FDA reports)
TONGUE COATED ( 4 FDA reports)
TONSILLITIS ( 4 FDA reports)
TOOTH INJURY ( 4 FDA reports)
TUMOUR PAIN ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
ABSCESS INTESTINAL ( 3 FDA reports)
ACIDOSIS ( 3 FDA reports)
ACUTE BIPHENOTYPIC LEUKAEMIA ( 3 FDA reports)
ACUTE LEUKAEMIA ( 3 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 3 FDA reports)
ACUTE MYELOMONOCYTIC LEUKAEMIA ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
ADENOVIRAL HAEMORRHAGIC CYSTITIS ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
ADVERSE REACTION ( 3 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ANORECTAL DISORDER ( 3 FDA reports)
AORTIC DISORDER ( 3 FDA reports)
APHERESIS ( 3 FDA reports)
ARTHROPOD BITE ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
AUTOIMMUNE DISORDER ( 3 FDA reports)
AUTOIMMUNE THYROIDITIS ( 3 FDA reports)
BACTERIA URINE IDENTIFIED ( 3 FDA reports)
BACTERIAL CULTURE POSITIVE ( 3 FDA reports)
BACTERIAL SEPSIS ( 3 FDA reports)
BACTEROIDES INFECTION ( 3 FDA reports)
BLINDNESS UNILATERAL ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 3 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 3 FDA reports)
BLOOD TEST ABNORMAL ( 3 FDA reports)
BLOOD URINE ( 3 FDA reports)
BODY MASS INDEX INCREASED ( 3 FDA reports)
BONE DENSITY INCREASED ( 3 FDA reports)
BONE MARROW ISCHAEMIA ( 3 FDA reports)
BONE MARROW OEDEMA ( 3 FDA reports)
BREAST CELLULITIS ( 3 FDA reports)
BREAST COSMETIC SURGERY ( 3 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 3 FDA reports)
BRONCHIOLITIS ( 3 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 3 FDA reports)
CAPILLARY LEAK SYNDROME ( 3 FDA reports)
CAROTID ARTERY OCCLUSION ( 3 FDA reports)
CATHETER SITE CELLULITIS ( 3 FDA reports)
CATHETER SITE INFECTION ( 3 FDA reports)
CATHETER SITE PAIN ( 3 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 3 FDA reports)
CEREBRAL CALCIFICATION ( 3 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 3 FDA reports)
CHEST WALL PAIN ( 3 FDA reports)
CHLAMYDIAL INFECTION ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 3 FDA reports)
CITROBACTER INFECTION ( 3 FDA reports)
CLUSTER HEADACHE ( 3 FDA reports)
COLON ADENOMA ( 3 FDA reports)
COLPORRHAPHY ( 3 FDA reports)
CONCUSSION ( 3 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 3 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
CYTOGENETIC ABNORMALITY ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
CYTOREDUCTIVE SURGERY ( 3 FDA reports)
DENTAL IMPLANTATION ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DEVICE MALFUNCTION ( 3 FDA reports)
DIABETIC KETOACIDOTIC HYPERGLYCAEMIC COMA ( 3 FDA reports)
DIPLEGIA ( 3 FDA reports)
DISEASE COMPLICATION ( 3 FDA reports)
DIZZINESS POSTURAL ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DYSPLASIA ( 3 FDA reports)
DYSPNOEA AT REST ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
ECONOMIC PROBLEM ( 3 FDA reports)
EJECTION FRACTION ABNORMAL ( 3 FDA reports)
EMBOLISM ( 3 FDA reports)
EMPYEMA ( 3 FDA reports)
ENCEPHALOMYELITIS ( 3 FDA reports)
ENCHONDROMA ( 3 FDA reports)
ENDOCARDIAL FIBROSIS ( 3 FDA reports)
ERYTHEMA MULTIFORME ( 3 FDA reports)
EWING'S SARCOMA ( 3 FDA reports)
EYE IRRITATION ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 3 FDA reports)
FOREIGN BODY REACTION ( 3 FDA reports)
FRACTURE ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GASTROINTESTINAL INFECTION ( 3 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 3 FDA reports)
GASTROSTOMY FAILURE ( 3 FDA reports)
GAZE PALSY ( 3 FDA reports)
GLOSSODYNIA ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 3 FDA reports)
GROWTH HORMONE DEFICIENCY ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEART VALVE INSUFFICIENCY ( 3 FDA reports)
HELICOBACTER INFECTION ( 3 FDA reports)
HEMIPLEGIA ( 3 FDA reports)
HEPATIC CONGESTION ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 3 FDA reports)
HYPERCOAGULATION ( 3 FDA reports)
HYPERMETROPIA ( 3 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 3 FDA reports)
HYPERURICAEMIA ( 3 FDA reports)
HYPOPROTEINAEMIA ( 3 FDA reports)
HYPOREFLEXIA ( 3 FDA reports)
INJECTION SITE BRUISING ( 3 FDA reports)
INJECTION SITE EXTRAVASATION ( 3 FDA reports)
INJECTION SITE SWELLING ( 3 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 3 FDA reports)
IRITIS ( 3 FDA reports)
IRON DEFICIENCY ( 3 FDA reports)
LEUKAEMIA RECURRENT ( 3 FDA reports)
LIP DRY ( 3 FDA reports)
LIVER TRANSPLANT ( 3 FDA reports)
LOCALISED OSTEOARTHRITIS ( 3 FDA reports)
LOWER LIMB FRACTURE ( 3 FDA reports)
LUNG ADENOCARCINOMA ( 3 FDA reports)
LYMPHANGITIS ( 3 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 3 FDA reports)
MALFORMATION VENOUS ( 3 FDA reports)
MASTOIDECTOMY ( 3 FDA reports)
MEDICAL DEVICE COMPLICATION ( 3 FDA reports)
MENIERE'S DISEASE ( 3 FDA reports)
MENINGEAL NEOPLASM ( 3 FDA reports)
MENINGITIS ASEPTIC ( 3 FDA reports)
METASTASES TO BLADDER ( 3 FDA reports)
MICROANGIOPATHY ( 3 FDA reports)
MUCOSAL ULCERATION ( 3 FDA reports)
MYCOSIS FUNGOIDES ( 3 FDA reports)
MYELOPATHY ( 3 FDA reports)
MYOPATHY STEROID ( 3 FDA reports)
NAIL DYSTROPHY ( 3 FDA reports)
NEUTROPENIC COLITIS ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
NODULE ON EXTREMITY ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
OPPORTUNISTIC INFECTION ( 3 FDA reports)
ORAL MUCOSAL DISORDER ( 3 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 3 FDA reports)
PARESIS ( 3 FDA reports)
PAROSMIA ( 3 FDA reports)
PELVIC ABSCESS ( 3 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 3 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 3 FDA reports)
PERIPHERAL NERVE LESION ( 3 FDA reports)
PLAGUE ( 3 FDA reports)
PLATELET DISORDER ( 3 FDA reports)
PLEURAL HAEMORRHAGE ( 3 FDA reports)
PO2 DECREASED ( 3 FDA reports)
POLYPECTOMY ( 3 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 3 FDA reports)
POST LAMINECTOMY SYNDROME ( 3 FDA reports)
POST-TRAUMATIC HEADACHE ( 3 FDA reports)
POSTOPERATIVE ADHESION ( 3 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
PREMATURE LABOUR ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PROCTITIS ( 3 FDA reports)
PULMONARY INTERSTITIAL EMPHYSEMA SYNDROME ( 3 FDA reports)
PYELONEPHRITIS ACUTE ( 3 FDA reports)
PYODERMA ( 3 FDA reports)
PYODERMA GANGRENOSUM ( 3 FDA reports)
RADIATION NECROSIS ( 3 FDA reports)
RASH PUSTULAR ( 3 FDA reports)
RECTAL ULCER ( 3 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 3 FDA reports)
RENAL INFARCT ( 3 FDA reports)
RESPIRATORY ALKALOSIS ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
RETROPERITONEAL HAEMATOMA ( 3 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 3 FDA reports)
RICKETS ( 3 FDA reports)
SCLERODERMA ( 3 FDA reports)
SERUM SICKNESS ( 3 FDA reports)
SKIN FRAGILITY ( 3 FDA reports)
SKIN TOXICITY ( 3 FDA reports)
SMALL FOR DATES BABY ( 3 FDA reports)
SOFT TISSUE INJURY ( 3 FDA reports)
SPLEEN DISORDER ( 3 FDA reports)
STATUS EPILEPTICUS ( 3 FDA reports)
STATUS MIGRAINOSUS ( 3 FDA reports)
STENT PLACEMENT ( 3 FDA reports)
TENSION HEADACHE ( 3 FDA reports)
TERATOMA ( 3 FDA reports)
TERMINAL STATE ( 3 FDA reports)
THYMUS ENLARGEMENT ( 3 FDA reports)
THYROID MASS ( 3 FDA reports)
THYROIDECTOMY ( 3 FDA reports)
TORUS FRACTURE ( 3 FDA reports)
TOXIC ENCEPHALOPATHY ( 3 FDA reports)
TOXIC NEUROPATHY ( 3 FDA reports)
TRANSPLANT ( 3 FDA reports)
TROPONIN INCREASED ( 3 FDA reports)
VAGINAL INFECTION ( 3 FDA reports)
VAGINOPLASTY ( 3 FDA reports)
VASCULAR PUNCTURE SITE SEALING ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
VIRAL MYOCARDITIS ( 3 FDA reports)
VITILIGO ( 3 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
ZYGOMYCOSIS ( 3 FDA reports)
ABDOMINAL HERNIA REPAIR ( 2 FDA reports)
ABDOMINAL INFECTION ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ABSCESS RUPTURE ( 2 FDA reports)
ACANTHOSIS ( 2 FDA reports)
ACCESSORY SPLEEN ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACID FAST BACILLI INFECTION ( 2 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 2 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
ACUTE PRERENAL FAILURE ( 2 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 2 FDA reports)
ADENOMYOSIS ( 2 FDA reports)
ADENOVIRAL HEPATITIS ( 2 FDA reports)
ADJUSTMENT DISORDER ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAEMIA NEONATAL ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANTITHROMBIN III DECREASED ( 2 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 2 FDA reports)
ANURIA ( 2 FDA reports)
APATHY ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTERIAL INSUFFICIENCY ( 2 FDA reports)
ATRIAL HYPERTROPHY ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 2 FDA reports)
AXILLARY VEIN THROMBOSIS ( 2 FDA reports)
AZOOSPERMIA ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BACTERIAL DISEASE CARRIER ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 2 FDA reports)
BIOPSY BREAST ( 2 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD GROWTH HORMONE DECREASED ( 2 FDA reports)
BLOOD INSULIN INCREASED ( 2 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BONE ABSCESS ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BRAIN COMPRESSION ( 2 FDA reports)
BRAIN DAMAGE ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
BRAIN STEM INFARCTION ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BRONCHIAL CARCINOMA ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CALCINOSIS ( 2 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 2 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 2 FDA reports)
CAROTID ARTERY THROMBOSIS ( 2 FDA reports)
CATHETER SITE DISCHARGE ( 2 FDA reports)
CATHETER SITE RELATED REACTION ( 2 FDA reports)
CELL-MEDIATED IMMUNE DEFICIENCY ( 2 FDA reports)
CELLULITIS GANGRENOUS ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CEREBELLAR TUMOUR ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBROSPINAL FLUID DRAINAGE ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHONDROSARCOMA ( 2 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 2 FDA reports)
CHRONIC FATIGUE SYNDROME ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
CLOSED FRACTURE MANIPULATION ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
COMPUTERISED TOMOGRAM CORONARY ARTERY ABNORMAL ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONJUNCTIVAL ABRASION ( 2 FDA reports)
CONTRALATERAL BREAST CANCER ( 2 FDA reports)
CONUS MEDULLARIS SYNDROME ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CORYNEBACTERIUM INFECTION ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CREST SYNDROME ( 2 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 2 FDA reports)
CYTOKINE STORM ( 2 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 2 FDA reports)
DANDRUFF ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DEGENERATION OF UTERINE LEIOMYOMA ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DENTAL DISCOMFORT ( 2 FDA reports)
DENTAL NECROSIS ( 2 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 2 FDA reports)
DEPRESSION SUICIDAL ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DERMATITIS ATOPIC ( 2 FDA reports)
DERMATITIS PSORIASIFORM ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG EFFECT PROLONGED ( 2 FDA reports)
DURAL TEAR ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSPAREUNIA ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ECZEMA NUMMULAR ( 2 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 2 FDA reports)
ENCEPHALITIS HERPES ( 2 FDA reports)
ENDOMETRIAL CANCER ( 2 FDA reports)
ENDOMETRIOSIS ( 2 FDA reports)
EPIDERMOLYSIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 2 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
ETHMOID SINUS SURGERY ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FAMILY STRESS ( 2 FDA reports)
FANCONI SYNDROME ACQUIRED ( 2 FDA reports)
FEBRILE CONVULSION ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FIBRINOLYSIS INCREASED ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
FUNGAEMIA ( 2 FDA reports)
FUNGAL SEPSIS ( 2 FDA reports)
GAMMA RADIATION THERAPY TO BRAIN ( 2 FDA reports)
GAS GANGRENE ( 2 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 2 FDA reports)
GASTRIC MUCOSAL LESION ( 2 FDA reports)
GASTRIC PERFORATION ( 2 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GENERALISED ANXIETY DISORDER ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GLIOSIS ( 2 FDA reports)
GLOBULINS INCREASED ( 2 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HAEMORRHAGIC DISORDER ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HERPES VIRUS INFECTION ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HIRSUTISM ( 2 FDA reports)
HISTOPLASMOSIS ( 2 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE UNSPECIFIED ( 2 FDA reports)
HOSTILITY ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
IIIRD NERVE PARALYSIS ( 2 FDA reports)
IMPAIRED FASTING GLUCOSE ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
IMPLANT SITE THROMBOSIS ( 2 FDA reports)
INCISION SITE COMPLICATION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INFECTED BITES ( 2 FDA reports)
INFUSION SITE PAIN ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INTENTION TREMOR ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
INTESTINAL INFARCTION ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
INTRACRANIAL HYPOTENSION ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
LASER THERAPY ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LIFE SUPPORT ( 2 FDA reports)
LOCKED-IN SYNDROME ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
MALIGNANT HYPERTENSION ( 2 FDA reports)
MANIA ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 2 FDA reports)
MELANODERMIA ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
METASTASES TO SKIN ( 2 FDA reports)
METASTASES TO SOFT TISSUE ( 2 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MONOCYTOSIS ( 2 FDA reports)
MONONEUROPATHY ( 2 FDA reports)
MUCOEPIDERMOID CARCINOMA ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MUSCLE NECROSIS ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
MYELOID MATURATION ARREST ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
MYOFASCITIS ( 2 FDA reports)
NAIL GROWTH ABNORMAL ( 2 FDA reports)
NEPHROBLASTOMA ( 2 FDA reports)
NEUROBLASTOMA ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NEUTROPENIA NEONATAL ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
ORAL MUCOSAL BLISTERING ( 2 FDA reports)
ORBITAL INFECTION ( 2 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 2 FDA reports)
ORTHOSTATIC TREMOR ( 2 FDA reports)
OSSICLE DISORDER ( 2 FDA reports)
OSTEITIS DEFORMANS ( 2 FDA reports)
OTOTOXICITY ( 2 FDA reports)
PAGET-SCHROETTER SYNDROME ( 2 FDA reports)
PAIN EXACERBATED ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PALLIATIVE CARE ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PARACENTESIS ( 2 FDA reports)
PARACENTESIS ABDOMEN ( 2 FDA reports)
PARATHYROID TUMOUR BENIGN ( 2 FDA reports)
PELVIC MASS ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHLEBOSCLEROSIS ( 2 FDA reports)
PIGMENTATION DISORDER ( 2 FDA reports)
PLASTIC SURGERY ( 2 FDA reports)
PLEURAL DISORDER ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONIA ASPERGILLUS ( 2 FDA reports)
PNEUMONIA CHLAMYDIAL ( 2 FDA reports)
PNEUMONIA INFLUENZAL ( 2 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 2 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 2 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 2 FDA reports)
PNEUMOPERICARDIUM ( 2 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
POSTOPERATIVE FEVER ( 2 FDA reports)
PRE-ECLAMPSIA ( 2 FDA reports)
PREMATURE DELIVERY ( 2 FDA reports)
PRIMITIVE NEUROECTODERMAL TUMOUR ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULMONARY ALVEOLAR MICROLITHIASIS ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
PURPURA ( 2 FDA reports)
PYOTHORAX ( 2 FDA reports)
QUADRIPARESIS ( 2 FDA reports)
RECALL PHENOMENON ( 2 FDA reports)
REHABILITATION THERAPY ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
SALMONELLA TEST POSITIVE ( 2 FDA reports)
SARCOMA ( 2 FDA reports)
SCAR EXCISION ( 2 FDA reports)
SENILE DEMENTIA ( 2 FDA reports)
SEPTIC EMBOLUS ( 2 FDA reports)
SEROMA ( 2 FDA reports)
SINUS ANTROSTOMY ( 2 FDA reports)
SKIN GRAFT ( 2 FDA reports)
SKIN ODOUR ABNORMAL ( 2 FDA reports)
SPINAL CORD HAEMORRHAGE ( 2 FDA reports)
SPINAL CORD NEOPLASM ( 2 FDA reports)
SPINAL OPERATION ( 2 FDA reports)
SPLENIC INFARCTION ( 2 FDA reports)
SPLENIC NECROSIS ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
SYNDACTYLY ( 2 FDA reports)
SYNOVIAL DISORDER ( 2 FDA reports)
SYRINGOMYELIA ( 2 FDA reports)
TEETH BRITTLE ( 2 FDA reports)
TENDON OPERATION ( 2 FDA reports)
TENOSYNOVITIS STENOSANS ( 2 FDA reports)
TRANSPLANT FAILURE ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TUMOUR NECROSIS ( 2 FDA reports)
TUMOUR PERFORATION ( 2 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 2 FDA reports)
ULCERATIVE KERATITIS ( 2 FDA reports)
UMBILICAL HERNIA REPAIR ( 2 FDA reports)
UTERINE CANCER ( 2 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 2 FDA reports)
VASCULAR STENOSIS ( 2 FDA reports)
VENOUS ANEURYSM ( 2 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 2 FDA reports)
VENTRICULAR HYPERKINESIA ( 2 FDA reports)
VOCAL CORD DISORDER ( 2 FDA reports)
WALKING DISABILITY ( 2 FDA reports)
WHOLE BLOOD TRANSFUSION ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
X-RAY DENTAL ( 2 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABDOMINAL WALL MASS ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABSCESS FUNGAL ( 1 FDA reports)
ABULIA ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACTINOMYCOTIC SKIN INFECTION ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ACUTE MEGAKARYOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE STRESS DISORDER ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADMINISTRATION SITE PAIN ( 1 FDA reports)
ADRENOCORTICAL CARCINOMA ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALLERGIC BRONCHITIS ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN DECREASED ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANAL INFLAMMATION ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 1 FDA reports)
ANGIOFIBROMA ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 1 FDA reports)
ANISEIKONIA ( 1 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 1 FDA reports)
ANTEROGRADE AMNESIA ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APOPTOSIS ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPLICATION SITE BRUISING ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BENCE JONES PROTEINURIA ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BLADDER CATHETERISATION ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
BLAST CELLS ( 1 FDA reports)
BLEPHAROPLASTY ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CARBON MONOXIDE ABNORMAL ( 1 FDA reports)
BLOOD COPPER INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INSPIRATORY DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD STEM CELL HARVEST FAILURE ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN MALFORMATION ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BUDD-CHIARI SYNDROME ( 1 FDA reports)
BULBAR PALSY ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
C-REACTIVE PROTEIN ( 1 FDA reports)
CALCIFICATION METASTATIC ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHEMICAL CYSTITIS ( 1 FDA reports)
CHEST WALL ABSCESS ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHROMOSOMAL MUTATION ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CHYLOTHORAX ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CIRRHOSIS ALCOHOLIC ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLECTOMY TOTAL ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLON GANGRENE ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COMMINUTED FRACTURE ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 1 FDA reports)
CONGENITAL HAND MALFORMATION ( 1 FDA reports)
CONGENITAL HERPES SIMPLEX INFECTION ( 1 FDA reports)
CONGENITAL NOSE MALFORMATION ( 1 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
COR PULMONALE ACUTE ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORNEAL ULCER ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CORYNEBACTERIUM SEPSIS ( 1 FDA reports)
COUGH DECREASED ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 1 FDA reports)
CSF CELL COUNT ABNORMAL ( 1 FDA reports)
CSF GLUCOSE ABNORMAL ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS TEST ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
CYTOTOXIC OEDEMA ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE II ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DUODENAL OBSTRUCTION ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMPHYSEMATOUS BULLA ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOCARDITIS NONINFECTIVE ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENDOTHELIAL DYSFUNCTION ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPIPHYSEAL DISORDER ( 1 FDA reports)
EPIPHYSIOLYSIS ( 1 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOMA ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYTHROBLAST COUNT NORMAL ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EWING'S SARCOMA METASTATIC ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYE ABSCESS ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEMALE GENITAL-DIGESTIVE TRACT FISTULA ( 1 FDA reports)
FEMALE ORGASMIC DISORDER ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUID REPLACEMENT ( 1 FDA reports)
FOETAL DEATH ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOETAL HEART RATE DISORDER ( 1 FDA reports)
FOETAL MOVEMENTS DECREASED ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FRACTURE MALUNION ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GANGLIONEUROMA ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GAUCHER'S DISEASE ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GINGIVAL ERYTHEMA ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GITELMAN'S SYNDROME ( 1 FDA reports)
GLIAL SCAR ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HAIRY CELL LEUKAEMIA ( 1 FDA reports)
HALITOSIS ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEARING AID USER ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC INFECTION FUNGAL ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATIC VEIN OCCLUSION ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS B VIRUS TEST ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HEPATOSPLENIC T-CELL LYMPHOMA ( 1 FDA reports)
HERPES OESOPHAGITIS ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIGH ARCHED PALATE ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HODGKIN'S DISEASE MIXED CELLULARITY RECURRENT ( 1 FDA reports)
HODGKIN'S DISEASE MIXED CELLULARITY STAGE IV ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYALURONIC ACID INCREASED ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPERMETABOLISM ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERVISCOSITY SYNDROME ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
ILEAL ULCER ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
IMPLANT SITE EXTRAVASATION ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPLANT SITE SWELLING ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFECTIVE THROMBOSIS ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INFUSION SITE BURNING ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INTERTRIGO ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JAW LESION EXCISION ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JEJUNAL ULCER ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KARYOTYPE ANALYSIS ABNORMAL ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
KUSSMAUL RESPIRATION ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEGIONELLA TEST ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LEUKOCORIA ( 1 FDA reports)
LEUKOSTASIS ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LIGHT CHAIN ANALYSIS ABNORMAL ( 1 FDA reports)
LIGHT CHAIN ANALYSIS DECREASED ( 1 FDA reports)
LIGHT CHAIN DISEASE ( 1 FDA reports)
LIMB DEFORMITY ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MALARIA ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MALIGNANT TRANSFORMATION ( 1 FDA reports)
MANTLE CELL LYMPHOMA ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEDICAL OBSERVATION ( 1 FDA reports)
MEDULLOBLASTOMA ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGOENCEPHALITIS HERPETIC ( 1 FDA reports)
MENINGORADICULITIS ( 1 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 1 FDA reports)
METASTASES TO BREAST ( 1 FDA reports)
METASTASES TO CHEST WALL ( 1 FDA reports)
METASTASES TO EYE ( 1 FDA reports)
METASTASES TO PELVIS ( 1 FDA reports)
METASTASES TO PERIPHERAL VASCULAR SYSTEM ( 1 FDA reports)
METASTASES TO SALIVARY GLAND ( 1 FDA reports)
METASTASES TO THYROID ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
MICROCEPHALY ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MULTIFOCAL MOTOR NEUROPATHY ( 1 FDA reports)
MULTIPLE GATED ACQUISITION SCAN ABNORMAL ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MYCOSIS FUNGOIDES RECURRENT ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
MYRINGOTOMY ( 1 FDA reports)
NAIL TOXICITY ( 1 FDA reports)
NASAL OBSTRUCTION ( 1 FDA reports)
NASAL SINUS CANCER ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUTROPHIL COUNT ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
OMENTECTOMY ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
ORAL CAVITY NEOPLASM SURGERY ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORAL NEOPLASM ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OSTECTOMY ( 1 FDA reports)
OSTEOCHONDROMA ( 1 FDA reports)
OSTEOMYELITIS ACUTE ( 1 FDA reports)
OSTEOTOMY ( 1 FDA reports)
OTOACOUSTIC EMISSIONS TEST ABNORMAL ( 1 FDA reports)
OVARIAN ENLARGEMENT ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANNICULITIS LOBULAR ( 1 FDA reports)
PARAINFLUENZAE VIRAL LARYNGOTRACHEOBRONCHITIS ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PERIPHERAL BLOOD STEM CELL APHERESIS ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED RECURRENT ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERITONEAL INFECTION ( 1 FDA reports)
PERITONEAL PERFORATION ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PLACENTA PRAEVIA ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLASMABLASTIC LYMPHOMA ( 1 FDA reports)
PLASMACYTOSIS ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PNEUMONIA ESCHERICHIA ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
PRECURSOR T-LYMPHOBLASTIC LYMPHOMA/LEUKAEMIA ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROCTOCOLITIS ( 1 FDA reports)
PROPHYLAXIS ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY MICROEMBOLI ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PYELOGRAM RETROGRADE ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
PYOMETRA ( 1 FDA reports)
RADIAL PULSE ABNORMAL ( 1 FDA reports)
RADIATION HEPATITIS ( 1 FDA reports)
RASH FOLLICULAR ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REMOVAL OF TRANSPLANTED ORGAN ( 1 FDA reports)
RENAL AMYLOIDOSIS ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RETICULOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RHABDOMYOSARCOMA ( 1 FDA reports)
RHABDOMYOSARCOMA RECURRENT ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RHYTHM IDIOVENTRICULAR ( 1 FDA reports)
RIGHT ATRIAL HYPERTROPHY ( 1 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCEDOSPORIUM INFECTION ( 1 FDA reports)
SCLERODACTYLIA ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SEBACEOUS CARCINOMA ( 1 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 1 FDA reports)
SELECTIVE IGA IMMUNODEFICIENCY ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SEROSITIS ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SINUSITIS BACTERIAL ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SOFT TISSUE MASS ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
SPINAL ANAESTHESIA ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STIFF-MAN SYNDROME ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPERINFECTION BACTERIAL ( 1 FDA reports)
SYMBOLIC DYSFUNCTION ( 1 FDA reports)
SYNOVIAL SARCOMA ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
T-CELL TYPE ACUTE LEUKAEMIA ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TACHYPHYLAXIS ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
THERAPEUTIC PROCEDURE ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THORACOTOMY ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TINEA CRURIS ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE DYSPLASIA ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TONSILLAR ULCER ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TRICHOSPORON INFECTION ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TROPONIN I ( 1 FDA reports)
TUMOUR COMPRESSION ( 1 FDA reports)
TUMOUR EMBOLISM ( 1 FDA reports)
TUMOUR EXCISION ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
UNDIFFERENTIATED SARCOMA ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URETERAL STENT INSERTION ( 1 FDA reports)
URETERIC HAEMORRHAGE ( 1 FDA reports)
URETHRAL OBSTRUCTION ( 1 FDA reports)
URETHRAL STENT INSERTION ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINARY TRACT PAIN ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
UROGENITAL DISORDER ( 1 FDA reports)
UROGRAM ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VIIITH NERVE LESION ( 1 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 1 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VOLVULUS OF BOWEL ( 1 FDA reports)
VULVAL CELLULITIS ( 1 FDA reports)
WEST NILE VIRAL INFECTION ( 1 FDA reports)
WHITE BLOOD CELL ANALYSIS INCREASED ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)

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