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

NAUSEA ( 17 FDA reports)
PAIN ( 14 FDA reports)
OSTEONECROSIS ( 13 FDA reports)
PYREXIA ( 13 FDA reports)
BONE DISORDER ( 12 FDA reports)
PAIN IN JAW ( 12 FDA reports)
VOMITING ( 12 FDA reports)
DYSPNOEA ( 11 FDA reports)
ANXIETY ( 10 FDA reports)
OSTEOMYELITIS ( 10 FDA reports)
OSTEONECROSIS OF JAW ( 10 FDA reports)
EJECTION FRACTION DECREASED ( 9 FDA reports)
FEBRILE NEUTROPENIA ( 9 FDA reports)
NEUTROPENIA ( 9 FDA reports)
ANAEMIA ( 8 FDA reports)
DIARRHOEA ( 8 FDA reports)
HEADACHE ( 8 FDA reports)
INFECTION ( 8 FDA reports)
INJURY ( 8 FDA reports)
MITRAL VALVE INCOMPETENCE ( 8 FDA reports)
PANCYTOPENIA ( 8 FDA reports)
PNEUMONIA ( 8 FDA reports)
TOOTH EXTRACTION ( 8 FDA reports)
CHEST PAIN ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
PLEURAL EFFUSION ( 7 FDA reports)
SWELLING ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
CARDIOMEGALY ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
IMPAIRED HEALING ( 6 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
SPINAL COMPRESSION FRACTURE ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
ASTHMA ( 5 FDA reports)
ATELECTASIS ( 5 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
FALL ( 5 FDA reports)
GASTRITIS ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 5 FDA reports)
LEUKOPENIA ( 5 FDA reports)
METASTASIS ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
NEUROPATHY PERIPHERAL ( 5 FDA reports)
ORAL SURGERY ( 5 FDA reports)
PERICARDIAL EFFUSION ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
RASH ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
TOOTHACHE ( 5 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
BREAST CANCER METASTATIC ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
DENTAL CARIES ( 4 FDA reports)
DIVERTICULUM INTESTINAL ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
EMOTIONAL DISTRESS ( 4 FDA reports)
FISTULA ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
GASTRIC POLYPS ( 4 FDA reports)
GINGIVAL INFECTION ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
HYPERLIPIDAEMIA ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
LOOSE TOOTH ( 4 FDA reports)
LYMPHADENOPATHY ( 4 FDA reports)
MASS ( 4 FDA reports)
METASTASES TO PERITONEUM ( 4 FDA reports)
MULTIPLE MYELOMA ( 4 FDA reports)
NEURALGIA ( 4 FDA reports)
ORAL PAIN ( 4 FDA reports)
ORTHOSTATIC HYPOTENSION ( 4 FDA reports)
OSTEOARTHRITIS ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PURULENT DISCHARGE ( 4 FDA reports)
RENAL CYST ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
SPINAL OSTEOARTHRITIS ( 4 FDA reports)
TOOTH DISORDER ( 4 FDA reports)
TOOTH LOSS ( 4 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
BONE DENSITY DECREASED ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
COLITIS ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DEATH ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
EROSIVE DUODENITIS ( 3 FDA reports)
FAILURE TO THRIVE ( 3 FDA reports)
GAMMA RADIATION THERAPY TO BRAIN ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
GINGIVAL SWELLING ( 3 FDA reports)
HAEMANGIOMA OF LIVER ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MASTICATION DISORDER ( 3 FDA reports)
METASTASES TO HEART ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
MYELOMA RECURRENCE ( 3 FDA reports)
OEDEMA MOUTH ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
OPEN FRACTURE ( 3 FDA reports)
ORAL DISCOMFORT ( 3 FDA reports)
ORAL INFECTION ( 3 FDA reports)
ORAL SOFT TISSUE DISORDER ( 3 FDA reports)
OSTEOLYSIS ( 3 FDA reports)
OSTEOPENIA ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RADIATION PNEUMONITIS ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
SOFT TISSUE INFECTION ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
THYMUS ENLARGEMENT ( 3 FDA reports)
TOOTH ABSCESS ( 3 FDA reports)
TOOTH FRACTURE ( 3 FDA reports)
TUMOUR MARKER INCREASED ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
ABSCESS ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BONE CYST ( 2 FDA reports)
BONE LESION ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
COMPRESSION FRACTURE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
GINGIVAL PAIN ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HYPERPLASIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
METASTASES TO PLEURA ( 2 FDA reports)
METASTATIC NEOPLASM ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
PRIMARY SEQUESTRUM ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RETINAL INFARCTION ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SOFT TISSUE DISORDER ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABSCESS NECK ( 1 FDA reports)
ACTINOMYCOSIS ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
APICECTOMY ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BIOPSY BONE ABNORMAL ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE FORMATION INCREASED ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRACHIAL PLEXOPATHY ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMYOPATHY ACUTE ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONJUNCTIVITIS VIRAL ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DEBRIDEMENT ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 1 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 1 FDA reports)
DENTAL OPERATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISSEMINATED LARGE CELL LYMPHOMA ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EDENTULOUS ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GINGIVAL EROSION ( 1 FDA reports)
GINGIVAL OEDEMA ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
INCISIONAL DRAINAGE ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
JAW OPERATION ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KYPHOSCOLIOSIS ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOCALISED OSTEOARTHRITIS ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MELANOSIS COLI ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO THE MEDIASTINUM ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MORGANELLA INFECTION ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYCOPLASMA TEST POSITIVE ( 1 FDA reports)
MYOCARDITIS BACTERIAL ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROTISING GASTRITIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NERVE BLOCK ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OMENTUM NEOPLASM ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL DISCHARGE ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OSTEORADIONECROSIS ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
OSTEOSYNTHESIS ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OTITIS MEDIA CHRONIC ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERIODONTAL DISEASE ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHYSICAL DISABILITY ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SEQUESTRECTOMY ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPLENIC CYST ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTH IMPACTED ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
URETHRAL CARUNCLE ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UTERINE ATONY ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
ZYGOMYCOSIS ( 1 FDA reports)

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