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

PAIN ( 31 FDA reports)
OSTEONECROSIS OF JAW ( 29 FDA reports)
ANXIETY ( 22 FDA reports)
BACK PAIN ( 20 FDA reports)
INJURY ( 20 FDA reports)
OSTEOMYELITIS ( 19 FDA reports)
ARTHRALGIA ( 17 FDA reports)
FATIGUE ( 17 FDA reports)
ANAEMIA ( 16 FDA reports)
PRIMARY SEQUESTRUM ( 16 FDA reports)
METASTASES TO LIVER ( 15 FDA reports)
PAIN IN JAW ( 15 FDA reports)
PARAESTHESIA ( 15 FDA reports)
BONE DISORDER ( 14 FDA reports)
DEPRESSION ( 13 FDA reports)
LYMPHADENOPATHY ( 13 FDA reports)
MUSCLE SPASMS ( 13 FDA reports)
NEOPLASM MALIGNANT ( 13 FDA reports)
DENTAL CARIES ( 12 FDA reports)
EMOTIONAL DISTRESS ( 12 FDA reports)
EXPOSED BONE IN JAW ( 12 FDA reports)
FALL ( 12 FDA reports)
HYPOAESTHESIA ( 12 FDA reports)
INFECTION ( 12 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 12 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 12 FDA reports)
NEUROPATHY PERIPHERAL ( 12 FDA reports)
PYREXIA ( 12 FDA reports)
CELLULITIS ( 11 FDA reports)
IMPAIRED HEALING ( 11 FDA reports)
OSTEOARTHRITIS ( 11 FDA reports)
POLYNEUROPATHY ( 11 FDA reports)
ACTINOMYCOSIS ( 10 FDA reports)
BONE PAIN ( 10 FDA reports)
EAR PAIN ( 10 FDA reports)
METASTASES TO SPINE ( 10 FDA reports)
NAUSEA ( 10 FDA reports)
OSTEOPOROSIS ( 10 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 10 FDA reports)
WEIGHT DECREASED ( 10 FDA reports)
ANHEDONIA ( 9 FDA reports)
CEREBROVASCULAR ACCIDENT ( 9 FDA reports)
DIARRHOEA ( 9 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 9 FDA reports)
SPINAL COMPRESSION FRACTURE ( 9 FDA reports)
SPINAL OSTEOARTHRITIS ( 9 FDA reports)
ASTHENIA ( 8 FDA reports)
BACTERIAL INFECTION ( 8 FDA reports)
CATARACT ( 8 FDA reports)
DECREASED INTEREST ( 8 FDA reports)
DISABILITY ( 8 FDA reports)
DIZZINESS ( 8 FDA reports)
DYSPNOEA ( 8 FDA reports)
DYSURIA ( 8 FDA reports)
ERYTHEMA ( 8 FDA reports)
FACIAL PAIN ( 8 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 8 FDA reports)
HEADACHE ( 8 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 8 FDA reports)
MUSCULOSKELETAL PAIN ( 8 FDA reports)
ORAL DISCOMFORT ( 8 FDA reports)
ORAL PAIN ( 8 FDA reports)
STAPHYLOCOCCAL INFECTION ( 8 FDA reports)
URINARY TRACT INFECTION ( 8 FDA reports)
ALOPECIA ( 7 FDA reports)
BRONCHITIS ( 7 FDA reports)
CONSTIPATION ( 7 FDA reports)
DIABETES MELLITUS ( 7 FDA reports)
DIVERTICULUM ( 7 FDA reports)
GAIT DISTURBANCE ( 7 FDA reports)
HAEMATURIA ( 7 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 7 FDA reports)
MASTICATION DISORDER ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
OSTEITIS ( 7 FDA reports)
OSTEOPENIA ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
PNEUMONIA ( 7 FDA reports)
RASH ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
SPLENOMEGALY ( 7 FDA reports)
SQUAMOUS CELL CARCINOMA ( 7 FDA reports)
SWELLING FACE ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
ATELECTASIS ( 6 FDA reports)
BONE MARROW FAILURE ( 6 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 6 FDA reports)
COUGH ( 6 FDA reports)
DECREASED APPETITE ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
DRY MOUTH ( 6 FDA reports)
DYSPHONIA ( 6 FDA reports)
FACET JOINT SYNDROME ( 6 FDA reports)
FRACTURE ( 6 FDA reports)
HAEMORRHOIDS ( 6 FDA reports)
HEPATIC STEATOSIS ( 6 FDA reports)
HYPERGLYCAEMIA ( 6 FDA reports)
INFLAMMATION ( 6 FDA reports)
ISCHAEMIA ( 6 FDA reports)
LACERATION ( 6 FDA reports)
LEUKOPENIA ( 6 FDA reports)
MALAISE ( 6 FDA reports)
METASTASES TO LUNG ( 6 FDA reports)
METASTASES TO PELVIS ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
NEUTROPENIA ( 6 FDA reports)
ORAL INFECTION ( 6 FDA reports)
OROPHARYNGEAL PAIN ( 6 FDA reports)
OSTEONECROSIS ( 6 FDA reports)
PURULENT DISCHARGE ( 6 FDA reports)
SINUSITIS ( 6 FDA reports)
VAGINAL INFECTION ( 6 FDA reports)
VISION BLURRED ( 6 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
ACUTE SINUSITIS ( 5 FDA reports)
BIOPSY ( 5 FDA reports)
BREAST CANCER RECURRENT ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
CHRONIC SINUSITIS ( 5 FDA reports)
DENTAL FISTULA ( 5 FDA reports)
DENTURE WEARER ( 5 FDA reports)
FOREIGN BODY IN EYE ( 5 FDA reports)
FUNGAL INFECTION ( 5 FDA reports)
GINGIVITIS ( 5 FDA reports)
GLARE ( 5 FDA reports)
HIATUS HERNIA ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
HYPOAESTHESIA ORAL ( 5 FDA reports)
HYPOKALAEMIA ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
JAW DISORDER ( 5 FDA reports)
LOOSE TOOTH ( 5 FDA reports)
METASTASES TO BONE ( 5 FDA reports)
MULTIPLE MYELOMA ( 5 FDA reports)
OEDEMA MOUTH ( 5 FDA reports)
ONYCHOMYCOSIS ( 5 FDA reports)
ORAL CANDIDIASIS ( 5 FDA reports)
ORTHOSTATIC HYPOTENSION ( 5 FDA reports)
OSTEORADIONECROSIS ( 5 FDA reports)
OSTEOSCLEROSIS ( 5 FDA reports)
PARESIS ( 5 FDA reports)
PATHOLOGICAL FRACTURE ( 5 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 5 FDA reports)
PRODUCTIVE COUGH ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
SCLEROMALACIA ( 5 FDA reports)
SWELLING ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
TOOTH ABSCESS ( 5 FDA reports)
TOOTHACHE ( 5 FDA reports)
TYPE 2 DIABETES MELLITUS ( 5 FDA reports)
URINARY RETENTION ( 5 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 5 FDA reports)
VISUAL ACUITY REDUCED ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
ARTHROPATHY ( 4 FDA reports)
BACTERIAL TEST POSITIVE ( 4 FDA reports)
BEDRIDDEN ( 4 FDA reports)
BLOOD CALCIUM DECREASED ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
COLONIC POLYP ( 4 FDA reports)
COMPRESSION FRACTURE ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
ERECTILE DYSFUNCTION ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
FOLLICULITIS ( 4 FDA reports)
GROIN PAIN ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
JOINT EFFUSION ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
KYPHOSIS ( 4 FDA reports)
LIGAMENT SPRAIN ( 4 FDA reports)
LUMBAR RADICULOPATHY ( 4 FDA reports)
LUNG NEOPLASM ( 4 FDA reports)
MONOCLONAL GAMMOPATHY ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
PLASMACYTOSIS ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
RASH PRURITIC ( 4 FDA reports)
RENAL CYST ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
RIB FRACTURE ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
SPONDYLOLISTHESIS ( 4 FDA reports)
SYNOVIAL CYST ( 4 FDA reports)
TENDONITIS ( 4 FDA reports)
TESTICULAR FAILURE ( 4 FDA reports)
THYROID NEOPLASM ( 4 FDA reports)
URETHRAL STENOSIS ( 4 FDA reports)
VOMITING ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABSCESS ( 3 FDA reports)
ABSCESS ORAL ( 3 FDA reports)
ADRENAL MASS ( 3 FDA reports)
AGEUSIA ( 3 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 3 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 3 FDA reports)
BONE CYST ( 3 FDA reports)
BONE FORMATION INCREASED ( 3 FDA reports)
BONE LESION ( 3 FDA reports)
BONE SCAN ABNORMAL ( 3 FDA reports)
BREAST ABSCESS ( 3 FDA reports)
BREAST ATROPHY ( 3 FDA reports)
BREATH ODOUR ( 3 FDA reports)
BURSITIS ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CYSTITIS NONINFECTIVE ( 3 FDA reports)
DEFORMITY ( 3 FDA reports)
DEMYELINATION ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
ESCHERICHIA INFECTION ( 3 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 3 FDA reports)
EXCORIATION ( 3 FDA reports)
FIBROSIS ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GASTROINTESTINAL PAIN ( 3 FDA reports)
GLIOSIS ( 3 FDA reports)
HAEMANGIOMA OF LIVER ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HEPATITIS C ( 3 FDA reports)
HIP FRACTURE ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HUMERUS FRACTURE ( 3 FDA reports)
HYDROCEPHALUS ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
HYPERLIPIDAEMIA ( 3 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 3 FDA reports)
IRRITABLE BOWEL SYNDROME ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LIP BLISTER ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
MASS ( 3 FDA reports)
METAPLASIA ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MYELOPATHY ( 3 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
NAIL DYSTROPHY ( 3 FDA reports)
NAIL INFECTION ( 3 FDA reports)
NASAL MUCOSAL DISORDER ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
NEOPLASM PROGRESSION ( 3 FDA reports)
NEOPLASM SKIN ( 3 FDA reports)
NEURALGIA ( 3 FDA reports)
NEURODERMATITIS ( 3 FDA reports)
NEUROFIBROMA ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
ONYCHALGIA ( 3 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 3 FDA reports)
ORTHOSIS USER ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PANCREATIC CYST ( 3 FDA reports)
PARONYCHIA ( 3 FDA reports)
PATELLA FRACTURE ( 3 FDA reports)
PERIODONTAL DISEASE ( 3 FDA reports)
PERIODONTITIS ( 3 FDA reports)
PERONEAL NERVE PALSY ( 3 FDA reports)
PLASMACYTOMA ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PROCEDURAL HYPERTENSION ( 3 FDA reports)
PROCTALGIA ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
PULMONARY FIBROSIS ( 3 FDA reports)
PULMONARY MASS ( 3 FDA reports)
PURULENCE ( 3 FDA reports)
PYELONEPHRITIS ACUTE ( 3 FDA reports)
RADICULAR PAIN ( 3 FDA reports)
RADICULITIS ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RHINITIS ALLERGIC ( 3 FDA reports)
RHINORRHOEA ( 3 FDA reports)
SALIVARY GLAND DISORDER ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
SKIN ATROPHY ( 3 FDA reports)
SPINAL COLUMN STENOSIS ( 3 FDA reports)
SPINAL CORD COMPRESSION ( 3 FDA reports)
SPINAL DISORDER ( 3 FDA reports)
SYNOVITIS ( 3 FDA reports)
TENDON DISORDER ( 3 FDA reports)
TENDON INJURY ( 3 FDA reports)
TOOTH DISORDER ( 3 FDA reports)
TOOTH LOSS ( 3 FDA reports)
TRACHEOBRONCHITIS ( 3 FDA reports)
TRIGEMINAL NEURALGIA ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
TUMOUR MARKER INCREASED ( 3 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
WALKING AID USER ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ACANTHOMA ( 2 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 2 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CATHETER SITE HAEMATOMA ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CYSTITIS HAEMORRHAGIC ( 2 FDA reports)
DEATH ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIABETIC FOOT ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSLIPIDAEMIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
DYSTHYMIC DISORDER ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
EXTERNAL EAR DISORDER ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GROIN ABSCESS ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HYDROURETER ( 2 FDA reports)
HYPERTONIC BLADDER ( 2 FDA reports)
JAW FRACTURE ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
MACULE ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
METASTASES TO SOFT TISSUE ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
OTITIS MEDIA ACUTE ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SINUS CONGESTION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SPINAL CLAUDICATION ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
THYROID CYST ( 2 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
ASCITES ( 1 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 1 FDA reports)
BIOPSY BONE MARROW ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYING ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENDOMETRIAL ATROPHY ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GIANT CELL TUMOUR OF TENDON SHEATH ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIFE EXPECTANCY SHORTENED ( 1 FDA reports)
LIGHT CHAIN ANALYSIS ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEDIASTINUM NEOPLASM ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NASAL OBSTRUCTION ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NODULE ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OS TRIGONUM SYNDROME ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OVARIAN MASS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARATHYROID TUMOUR BENIGN ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PHYSICAL DISABILITY ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTEIN URINE ABSENT ( 1 FDA reports)
PULMONARY AIR LEAKAGE ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
RADIATION OESOPHAGITIS ( 1 FDA reports)
RALES ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)

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