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

NAUSEA ( 77 FDA reports)
PAIN ( 72 FDA reports)
ANXIETY ( 64 FDA reports)
VOMITING ( 55 FDA reports)
BACK PAIN ( 54 FDA reports)
DIARRHOEA ( 54 FDA reports)
DEPRESSION ( 52 FDA reports)
DIZZINESS ( 52 FDA reports)
PNEUMONIA ( 51 FDA reports)
HEADACHE ( 50 FDA reports)
OEDEMA PERIPHERAL ( 50 FDA reports)
FATIGUE ( 49 FDA reports)
OSTEONECROSIS OF JAW ( 48 FDA reports)
WEIGHT DECREASED ( 46 FDA reports)
DYSPNOEA ( 42 FDA reports)
PAIN IN EXTREMITY ( 42 FDA reports)
ANAEMIA ( 41 FDA reports)
INSOMNIA ( 41 FDA reports)
FALL ( 40 FDA reports)
PYREXIA ( 40 FDA reports)
RASH ( 39 FDA reports)
OSTEOPENIA ( 38 FDA reports)
ABDOMINAL PAIN ( 37 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 36 FDA reports)
OSTEOPOROSIS ( 36 FDA reports)
URINARY TRACT INFECTION ( 36 FDA reports)
ASTHENIA ( 34 FDA reports)
DEEP VEIN THROMBOSIS ( 34 FDA reports)
INJURY ( 34 FDA reports)
ARTHRALGIA ( 33 FDA reports)
GAIT DISTURBANCE ( 33 FDA reports)
HYPERTENSION ( 33 FDA reports)
HYPOKALAEMIA ( 31 FDA reports)
SOMNOLENCE ( 31 FDA reports)
CONSTIPATION ( 30 FDA reports)
PAIN IN JAW ( 30 FDA reports)
HYPOAESTHESIA ( 29 FDA reports)
OSTEOARTHRITIS ( 29 FDA reports)
CHEST PAIN ( 27 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 27 FDA reports)
CONVULSION ( 27 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 27 FDA reports)
NEUROPATHY PERIPHERAL ( 27 FDA reports)
BRONCHITIS ( 26 FDA reports)
FEELING ABNORMAL ( 26 FDA reports)
PARAESTHESIA ( 26 FDA reports)
CANDIDIASIS ( 25 FDA reports)
DECREASED APPETITE ( 25 FDA reports)
DYSPHAGIA ( 25 FDA reports)
HYPONATRAEMIA ( 24 FDA reports)
MUSCLE SPASMS ( 24 FDA reports)
PULMONARY EMBOLISM ( 24 FDA reports)
METASTASES TO BONE ( 23 FDA reports)
THROMBOCYTOPENIA ( 23 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 22 FDA reports)
COUGH ( 22 FDA reports)
DEHYDRATION ( 22 FDA reports)
SPINAL OSTEOARTHRITIS ( 22 FDA reports)
CHOLELITHIASIS ( 21 FDA reports)
NEOPLASM MALIGNANT ( 21 FDA reports)
RENAL FAILURE ACUTE ( 21 FDA reports)
CARDIOMEGALY ( 20 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 20 FDA reports)
HAEMORRHOIDS ( 20 FDA reports)
TREMOR ( 20 FDA reports)
URTICARIA ( 20 FDA reports)
ASTHMA ( 19 FDA reports)
ATRIAL FIBRILLATION ( 19 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 19 FDA reports)
HYPERLIPIDAEMIA ( 19 FDA reports)
HYPOTENSION ( 19 FDA reports)
MALAISE ( 19 FDA reports)
OSTEOMYELITIS ( 19 FDA reports)
PLEURAL EFFUSION ( 19 FDA reports)
SLEEP APNOEA SYNDROME ( 19 FDA reports)
ANHEDONIA ( 18 FDA reports)
CELLULITIS ( 18 FDA reports)
CONFUSIONAL STATE ( 18 FDA reports)
DYSPEPSIA ( 18 FDA reports)
EXOSTOSIS ( 18 FDA reports)
INFECTION ( 18 FDA reports)
NEPHROLITHIASIS ( 18 FDA reports)
SEPSIS ( 18 FDA reports)
ATELECTASIS ( 17 FDA reports)
CARPAL TUNNEL SYNDROME ( 17 FDA reports)
CONDITION AGGRAVATED ( 17 FDA reports)
DIABETES MELLITUS ( 17 FDA reports)
DRUG INEFFECTIVE ( 17 FDA reports)
EMOTIONAL DISTRESS ( 17 FDA reports)
HIATUS HERNIA ( 17 FDA reports)
HYPERHIDROSIS ( 17 FDA reports)
OBESITY ( 17 FDA reports)
PANCYTOPENIA ( 17 FDA reports)
PRURITUS ( 17 FDA reports)
SINUSITIS ( 17 FDA reports)
ARRHYTHMIA ( 16 FDA reports)
ARTHRITIS ( 16 FDA reports)
BONE LESION ( 16 FDA reports)
DRUG INTERACTION ( 16 FDA reports)
FACIAL PAIN ( 16 FDA reports)
HEART RATE INCREASED ( 16 FDA reports)
HERPES ZOSTER ( 16 FDA reports)
IMPAIRED HEALING ( 16 FDA reports)
OEDEMA ( 16 FDA reports)
ORAL CANDIDIASIS ( 16 FDA reports)
SWELLING FACE ( 16 FDA reports)
VISION BLURRED ( 16 FDA reports)
BURSITIS ( 15 FDA reports)
CONTUSION ( 15 FDA reports)
MULTIPLE MYELOMA ( 15 FDA reports)
NECK PAIN ( 15 FDA reports)
OROPHARYNGEAL PAIN ( 15 FDA reports)
PALPITATIONS ( 15 FDA reports)
RENAL FAILURE CHRONIC ( 15 FDA reports)
SWELLING ( 15 FDA reports)
ABDOMINAL PAIN UPPER ( 14 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 14 FDA reports)
BONE DISORDER ( 14 FDA reports)
CEREBROVASCULAR ACCIDENT ( 14 FDA reports)
GINGIVAL PAIN ( 14 FDA reports)
HEAD INJURY ( 14 FDA reports)
HEPATIC STEATOSIS ( 14 FDA reports)
MUSCULAR WEAKNESS ( 14 FDA reports)
MUSCULOSKELETAL PAIN ( 14 FDA reports)
NEOPLASM PROGRESSION ( 14 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 14 FDA reports)
AGGRESSION ( 13 FDA reports)
CATARACT ( 13 FDA reports)
DYSPNOEA EXERTIONAL ( 13 FDA reports)
FOOT FRACTURE ( 13 FDA reports)
HYPERGLYCAEMIA ( 13 FDA reports)
PRODUCTIVE COUGH ( 13 FDA reports)
TENDONITIS ( 13 FDA reports)
TOOTH INFECTION ( 13 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
CARDIAC MURMUR ( 12 FDA reports)
CHEST DISCOMFORT ( 12 FDA reports)
CHRONIC SINUSITIS ( 12 FDA reports)
DENTAL CARIES ( 12 FDA reports)
DYSKINESIA ( 12 FDA reports)
EMOTIONAL DISORDER ( 12 FDA reports)
FEBRILE NEUTROPENIA ( 12 FDA reports)
FUNGAL INFECTION ( 12 FDA reports)
GINGIVAL BLEEDING ( 12 FDA reports)
HAEMATOCHEZIA ( 12 FDA reports)
JOINT SWELLING ( 12 FDA reports)
METABOLIC ACIDOSIS ( 12 FDA reports)
PLATELET COUNT DECREASED ( 12 FDA reports)
PNEUMOTHORAX ( 12 FDA reports)
POLLAKIURIA ( 12 FDA reports)
RIB FRACTURE ( 12 FDA reports)
SCOLIOSIS ( 12 FDA reports)
WEIGHT INCREASED ( 12 FDA reports)
AGRANULOCYTOSIS ( 11 FDA reports)
ALOPECIA ( 11 FDA reports)
BONE LOSS ( 11 FDA reports)
DEATH ( 11 FDA reports)
DYSPHONIA ( 11 FDA reports)
ERYTHEMA ( 11 FDA reports)
LYMPHOEDEMA ( 11 FDA reports)
MUCOSAL INFLAMMATION ( 11 FDA reports)
MUSCLE TWITCHING ( 11 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 11 FDA reports)
NEUTROPENIA ( 11 FDA reports)
NODULE ( 11 FDA reports)
OSTEITIS ( 11 FDA reports)
TOOTHACHE ( 11 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 11 FDA reports)
BALANCE DISORDER ( 10 FDA reports)
BLOOD PRESSURE INCREASED ( 10 FDA reports)
CATAPLEXY ( 10 FDA reports)
DISABILITY ( 10 FDA reports)
DRUG HYPERSENSITIVITY ( 10 FDA reports)
DYSURIA ( 10 FDA reports)
LOSS OF CONSCIOUSNESS ( 10 FDA reports)
MEMORY IMPAIRMENT ( 10 FDA reports)
MIGRAINE ( 10 FDA reports)
MITRAL VALVE INCOMPETENCE ( 10 FDA reports)
MYALGIA ( 10 FDA reports)
OSTEONECROSIS ( 10 FDA reports)
PULMONARY OEDEMA ( 10 FDA reports)
SINUS DISORDER ( 10 FDA reports)
SINUS TACHYCARDIA ( 10 FDA reports)
STOMATITIS ( 10 FDA reports)
SYNCOPE ( 10 FDA reports)
TENDERNESS ( 10 FDA reports)
TREATMENT NONCOMPLIANCE ( 10 FDA reports)
VISUAL IMPAIRMENT ( 10 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 10 FDA reports)
BONE PAIN ( 9 FDA reports)
COLITIS ( 9 FDA reports)
CORONARY ARTERY DISEASE ( 9 FDA reports)
DECREASED INTEREST ( 9 FDA reports)
DEFORMITY ( 9 FDA reports)
DIVERTICULUM INTESTINAL ( 9 FDA reports)
EXPOSED BONE IN JAW ( 9 FDA reports)
FLUID OVERLOAD ( 9 FDA reports)
GASTRITIS ( 9 FDA reports)
GOITRE ( 9 FDA reports)
HYPOTHYROIDISM ( 9 FDA reports)
ILEUS PARALYTIC ( 9 FDA reports)
INFLAMMATION ( 9 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 9 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 9 FDA reports)
LYMPHADENOPATHY ( 9 FDA reports)
MENTAL DISORDER ( 9 FDA reports)
OSTEOLYSIS ( 9 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 9 FDA reports)
ROAD TRAFFIC ACCIDENT ( 9 FDA reports)
SPINAL COMPRESSION FRACTURE ( 9 FDA reports)
STAPHYLOCOCCAL INFECTION ( 9 FDA reports)
TOOTH DISORDER ( 9 FDA reports)
ABSCESS ( 8 FDA reports)
ACETABULUM FRACTURE ( 8 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 8 FDA reports)
AORTIC VALVE INCOMPETENCE ( 8 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 8 FDA reports)
BLOOD GLUCOSE INCREASED ( 8 FDA reports)
CYST ( 8 FDA reports)
DEVICE MALFUNCTION ( 8 FDA reports)
DRUG EFFECT DECREASED ( 8 FDA reports)
ECONOMIC PROBLEM ( 8 FDA reports)
HAEMATURIA ( 8 FDA reports)
HORDEOLUM ( 8 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 8 FDA reports)
JAUNDICE ( 8 FDA reports)
KIDNEY INFECTION ( 8 FDA reports)
LEFT ATRIAL DILATATION ( 8 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 8 FDA reports)
LOCALISED INFECTION ( 8 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 8 FDA reports)
MENTAL STATUS CHANGES ( 8 FDA reports)
MOUTH ULCERATION ( 8 FDA reports)
MYOCARDIAL INFARCTION ( 8 FDA reports)
NERVOUSNESS ( 8 FDA reports)
OCULAR HYPERAEMIA ( 8 FDA reports)
OSTEOSCLEROSIS ( 8 FDA reports)
RASH PAPULAR ( 8 FDA reports)
RECTAL HAEMORRHAGE ( 8 FDA reports)
RECTAL POLYP ( 8 FDA reports)
RETCHING ( 8 FDA reports)
SEASONAL ALLERGY ( 8 FDA reports)
SOMNAMBULISM ( 8 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 8 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 8 FDA reports)
ABDOMINAL DISCOMFORT ( 7 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 7 FDA reports)
ARTHROPATHY ( 7 FDA reports)
BIPOLAR DISORDER ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 7 FDA reports)
BLOOD BILIRUBIN INCREASED ( 7 FDA reports)
BLOOD SODIUM DECREASED ( 7 FDA reports)
BONE MARROW FAILURE ( 7 FDA reports)
CHILLS ( 7 FDA reports)
CYSTITIS ( 7 FDA reports)
DEPRESSED MOOD ( 7 FDA reports)
DERMATITIS CONTACT ( 7 FDA reports)
DIVERTICULUM ( 7 FDA reports)
DRUG DOSE OMISSION ( 7 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 7 FDA reports)
DYSGEUSIA ( 7 FDA reports)
FACET JOINT SYNDROME ( 7 FDA reports)
FIBROSIS ( 7 FDA reports)
GINGIVAL ERYTHEMA ( 7 FDA reports)
GINGIVAL RECESSION ( 7 FDA reports)
GROIN PAIN ( 7 FDA reports)
HAEMATOMA ( 7 FDA reports)
HYPERMETABOLISM ( 7 FDA reports)
INJECTION SITE PAIN ( 7 FDA reports)
INTERSTITIAL LUNG DISEASE ( 7 FDA reports)
JAW FRACTURE ( 7 FDA reports)
LIGAMENT INJURY ( 7 FDA reports)
LUNG NEOPLASM ( 7 FDA reports)
LYMPHOMA ( 7 FDA reports)
MICTURITION URGENCY ( 7 FDA reports)
MIDDLE INSOMNIA ( 7 FDA reports)
MITRAL VALVE PROLAPSE ( 7 FDA reports)
MUMPS ( 7 FDA reports)
MYELOMA RECURRENCE ( 7 FDA reports)
NECK INJURY ( 7 FDA reports)
NIGHT SWEATS ( 7 FDA reports)
ORAL INFECTION ( 7 FDA reports)
PERSONALITY CHANGE ( 7 FDA reports)
PLEURAL FIBROSIS ( 7 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 7 FDA reports)
PRIMARY SEQUESTRUM ( 7 FDA reports)
RASH MORBILLIFORM ( 7 FDA reports)
RENAL FAILURE ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
RHEUMATOID ARTHRITIS ( 7 FDA reports)
RHINORRHOEA ( 7 FDA reports)
RUBELLA ( 7 FDA reports)
SCARLET FEVER ( 7 FDA reports)
SCIATICA ( 7 FDA reports)
SKIN DISORDER ( 7 FDA reports)
SKIN ODOUR ABNORMAL ( 7 FDA reports)
SKIN ULCER ( 7 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 7 FDA reports)
TENOSYNOVITIS STENOSANS ( 7 FDA reports)
TOOTH ABSCESS ( 7 FDA reports)
TOOTH FRACTURE ( 7 FDA reports)
TYPE 2 DIABETES MELLITUS ( 7 FDA reports)
URINARY INCONTINENCE ( 7 FDA reports)
VITAMIN D DECREASED ( 7 FDA reports)
ABDOMINAL PAIN LOWER ( 6 FDA reports)
ABNORMAL BEHAVIOUR ( 6 FDA reports)
ACTINOMYCOSIS ( 6 FDA reports)
ADRENAL INSUFFICIENCY ( 6 FDA reports)
AMNESIA ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 6 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
CARDIAC DISORDER ( 6 FDA reports)
CEREBRAL ATROPHY ( 6 FDA reports)
CERVICAL SPINAL STENOSIS ( 6 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 6 FDA reports)
COMMUNICATION DISORDER ( 6 FDA reports)
COMPRESSION FRACTURE ( 6 FDA reports)
CONJUNCTIVITIS ( 6 FDA reports)
CRYING ( 6 FDA reports)
DELIRIUM ( 6 FDA reports)
DEMENTIA ( 6 FDA reports)
DRY EYE ( 6 FDA reports)
DUODENITIS ( 6 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 6 FDA reports)
EYE PAIN ( 6 FDA reports)
FEELING HOT ( 6 FDA reports)
FOLLICULITIS ( 6 FDA reports)
GALLBLADDER DISORDER ( 6 FDA reports)
GLAUCOMA ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
HYPOPHAGIA ( 6 FDA reports)
HYPOPHOSPHATAEMIA ( 6 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 6 FDA reports)
LEUKOCYTOSIS ( 6 FDA reports)
LIVER DISORDER ( 6 FDA reports)
LOOSE TOOTH ( 6 FDA reports)
LUNG NEOPLASM MALIGNANT ( 6 FDA reports)
MALNUTRITION ( 6 FDA reports)
MASTICATION DISORDER ( 6 FDA reports)
ODYNOPHAGIA ( 6 FDA reports)
ORAL PAIN ( 6 FDA reports)
PNEUMONITIS ( 6 FDA reports)
PULMONARY CONGESTION ( 6 FDA reports)
PULMONARY FIBROSIS ( 6 FDA reports)
RASH ERYTHEMATOUS ( 6 FDA reports)
RENAL CYST ( 6 FDA reports)
ROTATOR CUFF SYNDROME ( 6 FDA reports)
SKIN BURNING SENSATION ( 6 FDA reports)
SKIN DISCOLOURATION ( 6 FDA reports)
SKIN LESION ( 6 FDA reports)
SUICIDAL IDEATION ( 6 FDA reports)
TARDIVE DYSKINESIA ( 6 FDA reports)
THIRST ( 6 FDA reports)
UPPER LIMB FRACTURE ( 6 FDA reports)
VERTIGO ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 5 FDA reports)
AORTIC VALVE SCLEROSIS ( 5 FDA reports)
BACTERIAL INFECTION ( 5 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
BREAST CANCER METASTATIC ( 5 FDA reports)
BURNING SENSATION ( 5 FDA reports)
CACHEXIA ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CARDIOMYOPATHY ( 5 FDA reports)
CHOLESTASIS ( 5 FDA reports)
COLONIC POLYP ( 5 FDA reports)
DEAFNESS ( 5 FDA reports)
DECUBITUS ULCER ( 5 FDA reports)
DIABETIC KETOACIDOSIS ( 5 FDA reports)
DIPLOPIA ( 5 FDA reports)
DISORIENTATION ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
DYSSTASIA ( 5 FDA reports)
ECZEMA ( 5 FDA reports)
EJECTION FRACTION DECREASED ( 5 FDA reports)
EMPHYSEMA ( 5 FDA reports)
EPISTAXIS ( 5 FDA reports)
EXTRASYSTOLES ( 5 FDA reports)
FOREIGN BODY ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HYPERCALCAEMIA ( 5 FDA reports)
HYPERTHYROIDISM ( 5 FDA reports)
HYPOACUSIS ( 5 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 5 FDA reports)
INCONTINENCE ( 5 FDA reports)
JOINT INJURY ( 5 FDA reports)
LARYNGITIS ( 5 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 5 FDA reports)
LETHARGY ( 5 FDA reports)
LEUKOPENIA ( 5 FDA reports)
LIGAMENT SPRAIN ( 5 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 5 FDA reports)
LIMB DISCOMFORT ( 5 FDA reports)
LUMBAR SPINAL STENOSIS ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
MALIGNANT MELANOMA ( 5 FDA reports)
MASS ( 5 FDA reports)
METASTASES TO SPINE ( 5 FDA reports)
NEUTROPHIL COUNT DECREASED ( 5 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 5 FDA reports)
ORAL HERPES ( 5 FDA reports)
PANCREATITIS ( 5 FDA reports)
PARAESTHESIA ORAL ( 5 FDA reports)
PELVIC PAIN ( 5 FDA reports)
PERICARDIAL EFFUSION ( 5 FDA reports)
PHARYNGITIS ( 5 FDA reports)
POOR QUALITY SLEEP ( 5 FDA reports)
PROTEINURIA ( 5 FDA reports)
PURULENT DISCHARGE ( 5 FDA reports)
RADICULOPATHY ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
RHINITIS ALLERGIC ( 5 FDA reports)
SLEEP DISORDER ( 5 FDA reports)
SLEEP-RELATED EATING DISORDER ( 5 FDA reports)
SPINAL COLUMN STENOSIS ( 5 FDA reports)
SPINAL DISORDER ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
STRESS ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
TONSILLITIS ( 5 FDA reports)
TRANSAMINASES INCREASED ( 5 FDA reports)
URINE OUTPUT DECREASED ( 5 FDA reports)
VAGINAL INFECTION ( 5 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
WITHDRAWAL SYNDROME ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
AIDS ENCEPHALOPATHY ( 4 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 4 FDA reports)
APHONIA ( 4 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
ARTERIOSCLEROSIS ( 4 FDA reports)
ASCITES ( 4 FDA reports)
ATAXIA ( 4 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 4 FDA reports)
BLINDNESS ( 4 FDA reports)
BONE SCAN ABNORMAL ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
CORNEAL DYSTROPHY ( 4 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 4 FDA reports)
DELUSION ( 4 FDA reports)
DERMATITIS ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
DYSTONIA ( 4 FDA reports)
EAR DISCOMFORT ( 4 FDA reports)
EAR PAIN ( 4 FDA reports)
ECCHYMOSIS ( 4 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 4 FDA reports)
EPICONDYLITIS ( 4 FDA reports)
EROSIVE OESOPHAGITIS ( 4 FDA reports)
EXCORIATION ( 4 FDA reports)
FAILURE TO THRIVE ( 4 FDA reports)
FEELING OF DESPAIR ( 4 FDA reports)
FIBROMYALGIA ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
FOOT DEFORMITY ( 4 FDA reports)
FUNGAL OESOPHAGITIS ( 4 FDA reports)
GANGRENE ( 4 FDA reports)
GASTRIC POLYPS ( 4 FDA reports)
GINGIVAL OEDEMA ( 4 FDA reports)
GINGIVITIS ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HALLUCINATION, VISUAL ( 4 FDA reports)
HEPATIC CYST ( 4 FDA reports)
HEPATOMEGALY ( 4 FDA reports)
HETEROTAXIA ( 4 FDA reports)
HIP FRACTURE ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
HYPERCOAGULATION ( 4 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 4 FDA reports)
ILEUS ( 4 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
INJECTION SITE ERYTHEMA ( 4 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 4 FDA reports)
INTESTINAL ULCER ( 4 FDA reports)
JOINT DISLOCATION ( 4 FDA reports)
KYPHOSIS ( 4 FDA reports)
LIP SWELLING ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
LOWER EXTREMITY MASS ( 4 FDA reports)
LUNG CANCER METASTATIC ( 4 FDA reports)
LYMPHOPENIA ( 4 FDA reports)
MENIERE'S DISEASE ( 4 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 4 FDA reports)
MOBILITY DECREASED ( 4 FDA reports)
MULTIPLE SCLEROSIS ( 4 FDA reports)
MUSCLE STRAIN ( 4 FDA reports)
MUSCLE TIGHTNESS ( 4 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
MYELODYSPLASTIC SYNDROME ( 4 FDA reports)
NARCOLEPSY ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
NEUROTOXICITY ( 4 FDA reports)
OESOPHAGEAL STENOSIS ( 4 FDA reports)
OVARIAN CYST ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PARAPROTEINAEMIA ( 4 FDA reports)
PARKINSON'S DISEASE ( 4 FDA reports)
PERIPHERAL COLDNESS ( 4 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 4 FDA reports)
PERONEAL NERVE PALSY ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
POST LAMINECTOMY SYNDROME ( 4 FDA reports)
PROSTATITIS ( 4 FDA reports)
PSORIASIS ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
PURULENCE ( 4 FDA reports)
RASH PRURITIC ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
RENAL ANEURYSM ( 4 FDA reports)
SCAB ( 4 FDA reports)
SCAR ( 4 FDA reports)
SEXUAL DYSFUNCTION ( 4 FDA reports)
SHOCK ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
SLEEP TALKING ( 4 FDA reports)
SLEEP TERROR ( 4 FDA reports)
SOFT TISSUE DISORDER ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
THROAT IRRITATION ( 4 FDA reports)
ULCER ( 4 FDA reports)
UNRESPONSIVE TO STIMULI ( 4 FDA reports)
URINE OUTPUT INCREASED ( 4 FDA reports)
VARICOSE VEIN ( 4 FDA reports)
VENOUS INSUFFICIENCY ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
WOUND ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 3 FDA reports)
ANKLE FRACTURE ( 3 FDA reports)
APHTHOUS STOMATITIS ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
ASTIGMATISM ( 3 FDA reports)
ATROPHIC VULVOVAGINITIS ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
BLINDNESS UNILATERAL ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 3 FDA reports)
BLOOD MAGNESIUM DECREASED ( 3 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
BONE DENSITY DECREASED ( 3 FDA reports)
BONE INFARCTION ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
BREAST MASS ( 3 FDA reports)
BREATH ODOUR ( 3 FDA reports)
BRUXISM ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CERUMEN IMPACTION ( 3 FDA reports)
CHOLECYSTITIS CHRONIC ( 3 FDA reports)
CHONDROMALACIA ( 3 FDA reports)
COLON CANCER ( 3 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 3 FDA reports)
CSF PRESSURE INCREASED ( 3 FDA reports)
CULTURE URINE POSITIVE ( 3 FDA reports)
CUTIS LAXA ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
DEMYELINATION ( 3 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 3 FDA reports)
DEVICE FAILURE ( 3 FDA reports)
DEVICE RELATED INFECTION ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DIABETIC NEUROPATHY ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DUODENAL POLYP ( 3 FDA reports)
DYSLIPIDAEMIA ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 3 FDA reports)
EYELID OEDEMA ( 3 FDA reports)
EYELID PTOSIS ( 3 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 3 FDA reports)
FISTULA ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
FORMICATION ( 3 FDA reports)
FURUNCLE ( 3 FDA reports)
GASTRITIS EROSIVE ( 3 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 3 FDA reports)
GINGIVAL INFECTION ( 3 FDA reports)
GLYCOSURIA ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
GRANULOCYTOPENIA ( 3 FDA reports)
GRANULOMA ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HEPATIC LESION ( 3 FDA reports)
HERPES SIMPLEX ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPERTONIC BLADDER ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
HYPOGONADISM ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
ILEITIS ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
INCREASED TENDENCY TO BRUISE ( 3 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
JOINT CREPITATION ( 3 FDA reports)
JOINT EFFUSION ( 3 FDA reports)
KYPHOSCOLIOSIS ( 3 FDA reports)
LIBIDO INCREASED ( 3 FDA reports)
LIFE EXPECTANCY SHORTENED ( 3 FDA reports)
LIPOMA ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
LOWER LIMB FRACTURE ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 3 FDA reports)
MARROW HYPERPLASIA ( 3 FDA reports)
MENOPAUSE ( 3 FDA reports)
MENORRHAGIA ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
METRORRHAGIA ( 3 FDA reports)
MOANING ( 3 FDA reports)
MOOD SWINGS ( 3 FDA reports)
MYOCLONUS ( 3 FDA reports)
MYOPATHY ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 3 FDA reports)
ONYCHOMYCOSIS ( 3 FDA reports)
OROMANDIBULAR DYSTONIA ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
OSTEORADIONECROSIS ( 3 FDA reports)
OTITIS MEDIA ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PAROTITIS ( 3 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 3 FDA reports)
PATHOLOGICAL FRACTURE ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
PRESBYOPIA ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
RADIUS FRACTURE ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
RETINAL TEAR ( 3 FDA reports)
RHINITIS ( 3 FDA reports)
SCLERITIS ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SKIN ATROPHY ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
SPONDYLOLISTHESIS ( 3 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
STREPTOCOCCAL SEPSIS ( 3 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 3 FDA reports)
SYNOVIAL CYST ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
TENDON DISORDER ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
TONGUE ULCERATION ( 3 FDA reports)
TRIGGER FINGER ( 3 FDA reports)
UTERINE LEIOMYOMA ( 3 FDA reports)
VAGINITIS BACTERIAL ( 3 FDA reports)
VENOUS THROMBOSIS LIMB ( 3 FDA reports)
VIITH NERVE PARALYSIS ( 3 FDA reports)
VITREOUS FLOATERS ( 3 FDA reports)
WALKING AID USER ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ABSCESS INTESTINAL ( 2 FDA reports)
ABSCESS NECK ( 2 FDA reports)
ABSCESS ORAL ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACNE ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ADDISON'S DISEASE ( 2 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
ANAL ULCER ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANOGENITAL WARTS ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 2 FDA reports)
ASPERGILLOSIS ORAL ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 2 FDA reports)
BIOPSY BONE ABNORMAL ( 2 FDA reports)
BIOPSY GINGIVAL ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
BITE ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLADDER OPERATION ( 2 FDA reports)
BLADDER PAIN ( 2 FDA reports)
BLADDER PROLAPSE ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD COPPER DECREASED ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 2 FDA reports)
BONE ATROPHY ( 2 FDA reports)
BONE CANCER METASTATIC ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BONE NEOPLASM MALIGNANT ( 2 FDA reports)
BREAST DISCHARGE ( 2 FDA reports)
BREAST HAEMATOMA ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
BULLOUS LUNG DISEASE ( 2 FDA reports)
BUNION ( 2 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 2 FDA reports)
CATARACT NUCLEAR ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONFABULATION ( 2 FDA reports)
CONJUNCTIVITIS VIRAL ( 2 FDA reports)
CONJUNCTIVOCHALASIS ( 2 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
DENTAL DISCOMFORT ( 2 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 2 FDA reports)
DENTAL PLAQUE ( 2 FDA reports)
DEPRESSIVE SYMPTOM ( 2 FDA reports)
DERMAL CYST ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DIABETIC FOOT ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DRUG TOLERANCE INCREASED ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 2 FDA reports)
DYSTHYMIC DISORDER ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
EDENTULOUS ( 2 FDA reports)
EJECTION FRACTION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EMPYEMA ( 2 FDA reports)
ENDOMETRIOSIS ( 2 FDA reports)
ENTEROVESICAL FISTULA ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
ESSENTIAL HYPERTENSION ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
EXOPHTHALMOS ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FAMILY STRESS ( 2 FDA reports)
FANCONI SYNDROME ( 2 FDA reports)
FAT TISSUE INCREASED ( 2 FDA reports)
FEELING DRUNK ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FIBROUS HISTIOCYTOMA ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
FOREIGN BODY REACTION ( 2 FDA reports)
FRACTURE NONUNION ( 2 FDA reports)
FRUSTRATION ( 2 FDA reports)
FUNGAEMIA ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GINGIVAL DISORDER ( 2 FDA reports)
GINGIVAL PRURITUS ( 2 FDA reports)
GLARE ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HAND FRACTURE ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
INAPPROPRIATE AFFECT ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCISION SITE INFECTION ( 2 FDA reports)
INFECTED SKIN ULCER ( 2 FDA reports)
INGROWING NAIL ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTERTRIGO ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
LYMPH NODE CALCIFICATION ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MAMMOPLASTY ( 2 FDA reports)
MANTLE CELL LYMPHOMA ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MELANOSIS COLI ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
METASTASES TO BONE MARROW ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
METASTASES TO MENINGES ( 2 FDA reports)
METASTATIC NEOPLASM ( 2 FDA reports)
METATARSUS PRIMUS VARUS ( 2 FDA reports)
MICROANGIOPATHY ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MYELITIS TRANSVERSE ( 2 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 2 FDA reports)
MYOFASCITIS ( 2 FDA reports)
MYOPIA ( 2 FDA reports)
NASAL OBSTRUCTION ( 2 FDA reports)
NECK MASS ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NEURODEGENERATIVE DISORDER ( 2 FDA reports)
NEURODERMATITIS ( 2 FDA reports)
NEUTROPENIC SEPSIS ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
OESOPHAGEAL DISORDER ( 2 FDA reports)
OESOPHAGEAL POLYP ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
ORAL CAVITY FISTULA ( 2 FDA reports)
ORAL DISCOMFORT ( 2 FDA reports)
ORAL PUSTULE ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OTITIS EXTERNA ( 2 FDA reports)
OTITIS MEDIA CHRONIC ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
OVARIAN DISORDER ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PELVIC ABSCESS ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PHYSICAL DISABILITY ( 2 FDA reports)
PITUITARY TUMOUR ( 2 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 2 FDA reports)
PLASMACYTOSIS ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
POLYHYDRAMNIOS ( 2 FDA reports)
POLYMYALGIA RHEUMATICA ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
POOR DENTAL CONDITION ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
POSTMENOPAUSE ( 2 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 2 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PULPITIS DENTAL ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
PYURIA ( 2 FDA reports)
QRS AXIS ABNORMAL ( 2 FDA reports)
RADIATION INJURY ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL MASS ( 2 FDA reports)
RESORPTION BONE INCREASED ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SEBORRHOEIC KERATOSIS ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SKIN CANDIDA ( 2 FDA reports)
SKIN FIBROSIS ( 2 FDA reports)
SKIN HYPERPIGMENTATION ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
SKIN PLAQUE ( 2 FDA reports)
SKIN TIGHTNESS ( 2 FDA reports)
SPINAL CORD OEDEMA ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
SPONDYLITIS ( 2 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 2 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
TEMPERATURE INTOLERANCE ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
THROMBOSIS IN DEVICE ( 2 FDA reports)
THYROID CYST ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
TUMOUR INVASION ( 2 FDA reports)
ULNAR NEURITIS ( 2 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 2 FDA reports)
URETHRAL CARUNCLE ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VARICOSE ULCERATION ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VOCAL CORD THICKENING ( 2 FDA reports)
VOMITING PROJECTILE ( 2 FDA reports)
VULVOVAGINAL PAIN ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 2 FDA reports)
X-RAY ABNORMAL ( 2 FDA reports)
ZYGOMYCOSIS ( 2 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABSCESS SWEAT GLAND ( 1 FDA reports)
ACANTHOMA ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACUTE LUNG INJURY ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
APATHY ( 1 FDA reports)
APPLICATION SITE PHOTOSENSITIVITY REACTION ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ASPIRATION BONE MARROW ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
AURA ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERIAL DIARRHOEA ( 1 FDA reports)
BACTERIAL DISEASE CARRIER ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BONE SCAN ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHITIS FUNGAL ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BULIMIA NERVOSA ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX INFECTION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CAMPYLOBACTER TEST POSITIVE ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CATHETER SITE SWELLING ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLESTASIS OF PREGNANCY ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CROUP INFECTIOUS ( 1 FDA reports)
CRYPTORCHISM ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVICE DAMAGE ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
EXTERNAL EAR CELLULITIS ( 1 FDA reports)
EXTERNAL EAR DISORDER ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE NAEVUS ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FEMALE ORGASMIC DISORDER ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOREIGN TRAVEL ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 1 FDA reports)
GENITAL INFECTION FUNGAL ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVAL EROSION ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS B DNA INCREASED ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HUMAN RHINOVIRUS TEST POSITIVE ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTRANSAMINASAEMIA ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFECTIVE TENOSYNOVITIS ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFUSION SITE SCAR ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INJURY CORNEAL ( 1 FDA reports)
INTERCOSTAL NEURALGIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
KELOID SCAR ( 1 FDA reports)
KERATOMILEUSIS ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LARYNGOCELE ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
LUMBAR SPINE FLATTENING ( 1 FDA reports)
LYMPHATIC DISORDER ( 1 FDA reports)
MACROSOMIA ( 1 FDA reports)
MACULAR FIBROSIS ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MACULE ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MANIA ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEGAKARYOCYTES INCREASED ( 1 FDA reports)
MEIBOMIANITIS ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MULTIFOCAL MOTOR NEUROPATHY ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 1 FDA reports)
NOONAN SYNDROME ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ONYCHALGIA ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PAPILLOMA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERIDIVERTICULAR ABSCESS ( 1 FDA reports)
PERIODONTAL DISEASE ( 1 FDA reports)
PERIORBITAL DISORDER ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PINGUECULA ( 1 FDA reports)
PIRIFORMIS SYNDROME ( 1 FDA reports)
PLAGUE ( 1 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 1 FDA reports)
PLEURODESIS ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
POUCHITIS ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PREGNANCY TEST POSITIVE ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PSYCHOTHERAPY ( 1 FDA reports)
PULMONARY AIR LEAKAGE ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RADICULAR PAIN ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL LIPOMATOSIS ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL OSTEODYSTROPHY ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RETICULOCYTOSIS ( 1 FDA reports)
RETINAL ARTERY THROMBOSIS ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCHAMBERG'S DISEASE ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SCROTAL IRRITATION ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SLEEP PARALYSIS ( 1 FDA reports)
SLOW SPEECH ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STARING ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STOMATOCYTES PRESENT ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TEETH BRITTLE ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
TENSION ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THORACIC OUTLET SYNDROME ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TINEA CRURIS ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
UTERINE CYST ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)
VAGINAL PROLAPSE ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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