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

DRUG INEFFECTIVE ( 233 FDA reports)
HYPERTENSION ( 162 FDA reports)
BLOOD PRESSURE INCREASED ( 145 FDA reports)
DIZZINESS ( 134 FDA reports)
FATIGUE ( 104 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 102 FDA reports)
NAUSEA ( 88 FDA reports)
ASTHENIA ( 86 FDA reports)
HEADACHE ( 83 FDA reports)
HYPOTENSION ( 82 FDA reports)
DRUG DOSE OMISSION ( 81 FDA reports)
VOMITING ( 81 FDA reports)
RENAL FAILURE ACUTE ( 80 FDA reports)
FALL ( 71 FDA reports)
DIARRHOEA ( 69 FDA reports)
MALAISE ( 69 FDA reports)
DYSPNOEA ( 66 FDA reports)
WEIGHT DECREASED ( 65 FDA reports)
OEDEMA PERIPHERAL ( 63 FDA reports)
PAIN ( 59 FDA reports)
DIABETES MELLITUS ( 58 FDA reports)
CEREBROVASCULAR ACCIDENT ( 57 FDA reports)
CHEST PAIN ( 57 FDA reports)
SYNCOPE ( 51 FDA reports)
ANAEMIA ( 50 FDA reports)
HYPONATRAEMIA ( 50 FDA reports)
RENAL FAILURE ( 49 FDA reports)
CARDIAC FAILURE ( 48 FDA reports)
MYOCARDIAL INFARCTION ( 47 FDA reports)
DEPRESSION ( 46 FDA reports)
BLOOD CREATININE INCREASED ( 45 FDA reports)
COUGH ( 45 FDA reports)
ANXIETY ( 44 FDA reports)
ARRHYTHMIA ( 42 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 42 FDA reports)
PAIN IN EXTREMITY ( 42 FDA reports)
INSOMNIA ( 41 FDA reports)
MYALGIA ( 41 FDA reports)
DRUG INTERACTION ( 39 FDA reports)
HYPOAESTHESIA ( 39 FDA reports)
MUSCLE SPASMS ( 38 FDA reports)
PYREXIA ( 38 FDA reports)
ARTHRALGIA ( 37 FDA reports)
DEHYDRATION ( 37 FDA reports)
PARAESTHESIA ( 37 FDA reports)
PNEUMONIA ( 36 FDA reports)
SOMNOLENCE ( 36 FDA reports)
ATRIAL FIBRILLATION ( 35 FDA reports)
LEUKOPENIA ( 31 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 30 FDA reports)
CORONARY ARTERY OCCLUSION ( 30 FDA reports)
CONFUSIONAL STATE ( 29 FDA reports)
HYPOTHYROIDISM ( 29 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 28 FDA reports)
WEIGHT INCREASED ( 28 FDA reports)
BACK PAIN ( 27 FDA reports)
BREAST CANCER ( 27 FDA reports)
BLOOD PRESSURE DECREASED ( 26 FDA reports)
ABDOMINAL PAIN ( 25 FDA reports)
ABDOMINAL PAIN UPPER ( 25 FDA reports)
DEEP VEIN THROMBOSIS ( 25 FDA reports)
GAIT DISTURBANCE ( 25 FDA reports)
NECK PAIN ( 25 FDA reports)
POLLAKIURIA ( 25 FDA reports)
BLOOD GLUCOSE INCREASED ( 24 FDA reports)
HYPERHIDROSIS ( 24 FDA reports)
PULMONARY OEDEMA ( 24 FDA reports)
TACHYCARDIA ( 24 FDA reports)
DYSPEPSIA ( 23 FDA reports)
EMOTIONAL DISTRESS ( 23 FDA reports)
THROMBOSIS ( 23 FDA reports)
INJURY ( 22 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 22 FDA reports)
CONDITION AGGRAVATED ( 21 FDA reports)
CONSTIPATION ( 21 FDA reports)
DRUG INTOLERANCE ( 21 FDA reports)
OFF LABEL USE ( 21 FDA reports)
OSTEOARTHRITIS ( 21 FDA reports)
VENOUS OCCLUSION ( 21 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 20 FDA reports)
HYPERCHOLESTEROLAEMIA ( 20 FDA reports)
INFARCTION ( 20 FDA reports)
LOSS OF CONSCIOUSNESS ( 20 FDA reports)
OEDEMA ( 20 FDA reports)
UNEVALUABLE EVENT ( 20 FDA reports)
VISION BLURRED ( 20 FDA reports)
VISUAL ACUITY REDUCED ( 20 FDA reports)
DEATH ( 19 FDA reports)
INFLUENZA ( 19 FDA reports)
ALOPECIA ( 18 FDA reports)
ANGINA PECTORIS ( 18 FDA reports)
ANHEDONIA ( 18 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 18 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 18 FDA reports)
MUSCULAR WEAKNESS ( 18 FDA reports)
OSTEONECROSIS ( 18 FDA reports)
PLEURAL EFFUSION ( 18 FDA reports)
PRURITUS ( 18 FDA reports)
RASH ( 18 FDA reports)
TOOTH EXTRACTION ( 18 FDA reports)
URINARY TRACT INFECTION ( 18 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 17 FDA reports)
FEELING ABNORMAL ( 17 FDA reports)
HEART RATE INCREASED ( 17 FDA reports)
LOWER LIMB FRACTURE ( 17 FDA reports)
PULMONARY EMBOLISM ( 17 FDA reports)
TINNITUS ( 17 FDA reports)
UPPER LIMB FRACTURE ( 17 FDA reports)
ASTHMA ( 16 FDA reports)
BONE DISORDER ( 16 FDA reports)
BRADYCARDIA ( 16 FDA reports)
DECREASED APPETITE ( 16 FDA reports)
ERYTHEMA ( 16 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 16 FDA reports)
HYPERTENSIVE CRISIS ( 16 FDA reports)
NASOPHARYNGITIS ( 16 FDA reports)
NEUTROPENIA ( 16 FDA reports)
RENAL IMPAIRMENT ( 16 FDA reports)
SWELLING FACE ( 16 FDA reports)
TREMOR ( 16 FDA reports)
VERTIGO ( 16 FDA reports)
ANKLE FRACTURE ( 15 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 15 FDA reports)
BLOOD SODIUM DECREASED ( 15 FDA reports)
BRONCHITIS ( 15 FDA reports)
GOUT ( 15 FDA reports)
HYPOKALAEMIA ( 15 FDA reports)
HYPOKINESIA ( 15 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 15 FDA reports)
MEMORY IMPAIRMENT ( 15 FDA reports)
PALPITATIONS ( 15 FDA reports)
RESPIRATORY FAILURE ( 15 FDA reports)
SWELLING ( 15 FDA reports)
THROMBOCYTOPENIA ( 15 FDA reports)
TOOTH LOSS ( 15 FDA reports)
ABASIA ( 14 FDA reports)
AMNESIA ( 14 FDA reports)
BURNING SENSATION ( 14 FDA reports)
CARDIAC DISORDER ( 14 FDA reports)
DRY MOUTH ( 14 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 14 FDA reports)
GASTRITIS ( 14 FDA reports)
INCORRECT DOSE ADMINISTERED ( 14 FDA reports)
INTENTIONAL DRUG MISUSE ( 14 FDA reports)
MENTAL DISORDER ( 14 FDA reports)
MITRAL VALVE INCOMPETENCE ( 14 FDA reports)
OBESITY ( 14 FDA reports)
OLIGURIA ( 14 FDA reports)
OSTEOPOROSIS ( 14 FDA reports)
PAIN IN JAW ( 14 FDA reports)
PRURITUS GENERALISED ( 14 FDA reports)
SINUSITIS ( 14 FDA reports)
SWOLLEN TONGUE ( 14 FDA reports)
ARTHRITIS ( 13 FDA reports)
BONE OPERATION ( 13 FDA reports)
CARDIAC ARREST ( 13 FDA reports)
CARDIOMEGALY ( 13 FDA reports)
DRUG DISPENSING ERROR ( 13 FDA reports)
GASTRIC ULCER ( 13 FDA reports)
INTERSTITIAL LUNG DISEASE ( 13 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 13 FDA reports)
LIVER INJURY ( 13 FDA reports)
LOCAL SWELLING ( 13 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 13 FDA reports)
PULMONARY HYPERTENSION ( 13 FDA reports)
SCAR ( 13 FDA reports)
ADVERSE EVENT ( 12 FDA reports)
BALANCE DISORDER ( 12 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 12 FDA reports)
CHEST DISCOMFORT ( 12 FDA reports)
DRUG HYPERSENSITIVITY ( 12 FDA reports)
DRUG PRESCRIBING ERROR ( 12 FDA reports)
HEPATIC STEATOSIS ( 12 FDA reports)
OSTEOMYELITIS ( 12 FDA reports)
PANCREATITIS ( 12 FDA reports)
RENAL CYST ( 12 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 12 FDA reports)
VISUAL IMPAIRMENT ( 12 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 12 FDA reports)
ANOREXIA ( 11 FDA reports)
CATARACT ( 11 FDA reports)
CHILLS ( 11 FDA reports)
CHOLELITHIASIS ( 11 FDA reports)
EPISTAXIS ( 11 FDA reports)
FEELING HOT ( 11 FDA reports)
FEMUR FRACTURE ( 11 FDA reports)
HAEMOGLOBIN DECREASED ( 11 FDA reports)
JOINT SWELLING ( 11 FDA reports)
MEDICATION ERROR ( 11 FDA reports)
MUSCULOSKELETAL PAIN ( 11 FDA reports)
NEPHROLITHIASIS ( 11 FDA reports)
PAROTID GLAND ENLARGEMENT ( 11 FDA reports)
SINUSITIS FUNGAL ( 11 FDA reports)
SLEEP DISORDER ( 11 FDA reports)
AORTIC VALVE INCOMPETENCE ( 10 FDA reports)
CARDIAC MURMUR ( 10 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 10 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 10 FDA reports)
FEAR ( 10 FDA reports)
HAEMORRHOIDS ( 10 FDA reports)
ILL-DEFINED DISORDER ( 10 FDA reports)
INFECTION ( 10 FDA reports)
LIMB CRUSHING INJURY ( 10 FDA reports)
LUMBAR RADICULOPATHY ( 10 FDA reports)
NERVOUSNESS ( 10 FDA reports)
NEUROPATHY PERIPHERAL ( 10 FDA reports)
OROPHARYNGEAL PAIN ( 10 FDA reports)
PRESYNCOPE ( 10 FDA reports)
PROCEDURAL PAIN ( 10 FDA reports)
PROSTATE CANCER ( 10 FDA reports)
RENAL INJURY ( 10 FDA reports)
SEPTIC SHOCK ( 10 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 10 FDA reports)
ADVERSE DRUG REACTION ( 9 FDA reports)
BLINDNESS ( 9 FDA reports)
BLOOD BILIRUBIN INCREASED ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 9 FDA reports)
BLOOD PRESSURE ABNORMAL ( 9 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 9 FDA reports)
CARPAL TUNNEL SYNDROME ( 9 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 9 FDA reports)
CEREBRAL INFARCTION ( 9 FDA reports)
COLITIS ( 9 FDA reports)
DILATATION VENTRICULAR ( 9 FDA reports)
DYSURIA ( 9 FDA reports)
EYE SWELLING ( 9 FDA reports)
FLUID RETENTION ( 9 FDA reports)
HYPERGLYCAEMIA ( 9 FDA reports)
MACULAR DEGENERATION ( 9 FDA reports)
PALLOR ( 9 FDA reports)
PROTHROMBIN TIME SHORTENED ( 9 FDA reports)
RASH MACULAR ( 9 FDA reports)
TRANSFUSION ( 9 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 9 FDA reports)
URINARY INCONTINENCE ( 9 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 8 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 8 FDA reports)
CAROTID BRUIT ( 8 FDA reports)
CHROMATURIA ( 8 FDA reports)
COAGULOPATHY ( 8 FDA reports)
CORONARY ARTERY STENOSIS ( 8 FDA reports)
DEBRIDEMENT ( 8 FDA reports)
DISORIENTATION ( 8 FDA reports)
DYSPHONIA ( 8 FDA reports)
FISTULA ( 8 FDA reports)
FOOT FRACTURE ( 8 FDA reports)
HEPATIC ENZYME INCREASED ( 8 FDA reports)
HUMERUS FRACTURE ( 8 FDA reports)
HYPERSENSITIVITY ( 8 FDA reports)
HYPOGLYCAEMIA ( 8 FDA reports)
INFLUENZA LIKE ILLNESS ( 8 FDA reports)
LETHARGY ( 8 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 8 FDA reports)
LUNG NEOPLASM ( 8 FDA reports)
MELAENA ( 8 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 8 FDA reports)
PERICARDIAL EFFUSION ( 8 FDA reports)
RADIUS FRACTURE ( 8 FDA reports)
SEPSIS ( 8 FDA reports)
THROAT IRRITATION ( 8 FDA reports)
URINE OUTPUT DECREASED ( 8 FDA reports)
ABDOMINAL DISTENSION ( 7 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 7 FDA reports)
AGITATION ( 7 FDA reports)
BLOOD POTASSIUM INCREASED ( 7 FDA reports)
BLOOD UREA INCREASED ( 7 FDA reports)
CELLULITIS ( 7 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 7 FDA reports)
COMA ( 7 FDA reports)
DENTAL CARIES ( 7 FDA reports)
EJECTION FRACTION DECREASED ( 7 FDA reports)
EYE PRURITUS ( 7 FDA reports)
EYELID OEDEMA ( 7 FDA reports)
FLUSHING ( 7 FDA reports)
GLAUCOMA ( 7 FDA reports)
HAEMATOCRIT DECREASED ( 7 FDA reports)
HEPATOMEGALY ( 7 FDA reports)
HYDRONEPHROSIS ( 7 FDA reports)
HYPERKALAEMIA ( 7 FDA reports)
HYPOVOLAEMIC SHOCK ( 7 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 7 FDA reports)
MIGRAINE ( 7 FDA reports)
NERVE COMPRESSION ( 7 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 7 FDA reports)
RENAL COLIC ( 7 FDA reports)
RENAL FAILURE CHRONIC ( 7 FDA reports)
RIB FRACTURE ( 7 FDA reports)
SKIN CANCER ( 7 FDA reports)
SQUAMOUS CELL CARCINOMA ( 7 FDA reports)
STREPTOCOCCAL INFECTION ( 7 FDA reports)
STRESS ( 7 FDA reports)
TREATMENT NONCOMPLIANCE ( 7 FDA reports)
ABDOMINAL DISCOMFORT ( 6 FDA reports)
ACUTE PRERENAL FAILURE ( 6 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
ASTIGMATISM ( 6 FDA reports)
BLOOD GLUCOSE DECREASED ( 6 FDA reports)
BONE PAIN ( 6 FDA reports)
BRONCHOSPASM ( 6 FDA reports)
CARDIOVASCULAR DISORDER ( 6 FDA reports)
CEREBRAL ISCHAEMIA ( 6 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 6 FDA reports)
CONTUSION ( 6 FDA reports)
CORONARY ARTERY DISEASE ( 6 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 6 FDA reports)
DRUG EFFECT DECREASED ( 6 FDA reports)
DRY EYE ( 6 FDA reports)
DUODENAL ULCER ( 6 FDA reports)
DYSGEUSIA ( 6 FDA reports)
EXOSTOSIS ( 6 FDA reports)
EYE DISORDER ( 6 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 6 FDA reports)
GINGIVAL EROSION ( 6 FDA reports)
HYPERLIPIDAEMIA ( 6 FDA reports)
HYPERMETROPIA ( 6 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 6 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 6 FDA reports)
ISCHAEMIC STROKE ( 6 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 6 FDA reports)
LACRIMATION DECREASED ( 6 FDA reports)
LUDWIG ANGINA ( 6 FDA reports)
LUNG NEOPLASM MALIGNANT ( 6 FDA reports)
LYMPHADENITIS ( 6 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
MULTIPLE INJURIES ( 6 FDA reports)
NASAL CONGESTION ( 6 FDA reports)
NEOPLASM MALIGNANT ( 6 FDA reports)
NOSOCOMIAL INFECTION ( 6 FDA reports)
OCULAR ICTERUS ( 6 FDA reports)
OEDEMA MOUTH ( 6 FDA reports)
PETECHIAE ( 6 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 6 FDA reports)
PNEUMONIA ASPIRATION ( 6 FDA reports)
PSORIASIS ( 6 FDA reports)
RESTLESSNESS ( 6 FDA reports)
ROAD TRAFFIC ACCIDENT ( 6 FDA reports)
SPEECH DISORDER ( 6 FDA reports)
SPINAL COLUMN STENOSIS ( 6 FDA reports)
SUBILEUS ( 6 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 6 FDA reports)
TRACHEOSTOMY ( 6 FDA reports)
URINE OUTPUT INCREASED ( 6 FDA reports)
VITREOUS FLOATERS ( 6 FDA reports)
ABSCESS ( 5 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 5 FDA reports)
ANGIOPLASTY ( 5 FDA reports)
AORTIC ANEURYSM ( 5 FDA reports)
BEDRIDDEN ( 5 FDA reports)
BLOOD CREATININE DECREASED ( 5 FDA reports)
BLOOD URIC ACID INCREASED ( 5 FDA reports)
CARDIAC PACEMAKER INSERTION ( 5 FDA reports)
CAROTID ARTERY OCCLUSION ( 5 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 5 FDA reports)
CERVICOBRACHIAL SYNDROME ( 5 FDA reports)
CHOLECYSTITIS ( 5 FDA reports)
COGNITIVE DISORDER ( 5 FDA reports)
DYSLIPIDAEMIA ( 5 FDA reports)
ECZEMA ( 5 FDA reports)
EMOTIONAL DISORDER ( 5 FDA reports)
ERYTHEMA MULTIFORME ( 5 FDA reports)
FAECES DISCOLOURED ( 5 FDA reports)
GASTROINTESTINAL DISORDER ( 5 FDA reports)
GINGIVITIS ( 5 FDA reports)
GLOSSODYNIA ( 5 FDA reports)
HEMIPARESIS ( 5 FDA reports)
IMPAIRED HEALING ( 5 FDA reports)
INJECTION SITE ERYTHEMA ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
JOINT EFFUSION ( 5 FDA reports)
LABORATORY TEST ABNORMAL ( 5 FDA reports)
LIMB DISCOMFORT ( 5 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 5 FDA reports)
MASTECTOMY ( 5 FDA reports)
MICTURITION URGENCY ( 5 FDA reports)
MULTIPLE SCLEROSIS ( 5 FDA reports)
MUSCLE CRAMP ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
NIGHT SWEATS ( 5 FDA reports)
OESOPHAGITIS ( 5 FDA reports)
OSTEONECROSIS OF JAW ( 5 FDA reports)
PNEUMOTHORAX ( 5 FDA reports)
POLYNEUROPATHY ( 5 FDA reports)
PULMONARY FIBROSIS ( 5 FDA reports)
RASH GENERALISED ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
RESPIRATORY TRACT INFECTION ( 5 FDA reports)
RHEUMATOID ARTHRITIS ( 5 FDA reports)
RHINITIS ALLERGIC ( 5 FDA reports)
SENSATION OF HEAVINESS ( 5 FDA reports)
SENSORY LOSS ( 5 FDA reports)
STENT PLACEMENT ( 5 FDA reports)
THROAT LESION ( 5 FDA reports)
THYROID NEOPLASM ( 5 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
URINE ODOUR ABNORMAL ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
VASCULAR GRAFT ( 5 FDA reports)
VENTRICULAR DYSFUNCTION ( 5 FDA reports)
VISUAL DISTURBANCE ( 5 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
WOUND ( 5 FDA reports)
WRONG DRUG ADMINISTERED ( 5 FDA reports)
YELLOW SKIN ( 5 FDA reports)
ALBUMIN URINE PRESENT ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ANGINA UNSTABLE ( 4 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 4 FDA reports)
AORTIC VALVE SCLEROSIS ( 4 FDA reports)
APHAGIA ( 4 FDA reports)
ARTERIOSCLEROSIS ( 4 FDA reports)
ATRIAL FLUTTER ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 4 FDA reports)
BACK INJURY ( 4 FDA reports)
BLOOD CULTURE POSITIVE ( 4 FDA reports)
BLOOD URINE PRESENT ( 4 FDA reports)
BONE DENSITY DECREASED ( 4 FDA reports)
BREAST MASS ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 4 FDA reports)
CRYING ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
DIVERTICULITIS ( 4 FDA reports)
DIVERTICULUM ( 4 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 4 FDA reports)
DRUG DEPENDENCE ( 4 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 4 FDA reports)
DYSPAREUNIA ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
ERECTILE DYSFUNCTION ( 4 FDA reports)
EXCORIATION ( 4 FDA reports)
EXTRASYSTOLES ( 4 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
FIBROMYALGIA ( 4 FDA reports)
FLATULENCE ( 4 FDA reports)
GASTRIC DISORDER ( 4 FDA reports)
GASTRIC HAEMORRHAGE ( 4 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 4 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HEPATIC ENZYME ABNORMAL ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
HYPERVENTILATION ( 4 FDA reports)
HYPOPHAGIA ( 4 FDA reports)
INJECTION SITE HAEMORRHAGE ( 4 FDA reports)
INJECTION SITE REACTION ( 4 FDA reports)
INJECTION SITE THROMBOSIS ( 4 FDA reports)
INTERVERTEBRAL DISCITIS ( 4 FDA reports)
INTESTINAL STENOSIS ( 4 FDA reports)
ISCHAEMIA ( 4 FDA reports)
JAW DISORDER ( 4 FDA reports)
LYMPHADENECTOMY ( 4 FDA reports)
MEDICATION RESIDUE ( 4 FDA reports)
MENSTRUATION IRREGULAR ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
MICROALBUMINURIA ( 4 FDA reports)
MIDDLE INSOMNIA ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
MUSCLE RIGIDITY ( 4 FDA reports)
NASAL DRYNESS ( 4 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 4 FDA reports)
NERVE INJURY ( 4 FDA reports)
NIGHTMARE ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
PRODUCTIVE COUGH ( 4 FDA reports)
PROSTATOMEGALY ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
PULMONARY CONGESTION ( 4 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 4 FDA reports)
RECTAL CANCER ( 4 FDA reports)
RENAL ARTERY OCCLUSION ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
SALPINGITIS ( 4 FDA reports)
SCIATICA ( 4 FDA reports)
SICK SINUS SYNDROME ( 4 FDA reports)
SKIN BURNING SENSATION ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
SLEEP APNOEA SYNDROME ( 4 FDA reports)
SPINAL OSTEOARTHRITIS ( 4 FDA reports)
STOMACH DISCOMFORT ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
THROMBOPHLEBITIS ( 4 FDA reports)
TONGUE DISORDER ( 4 FDA reports)
TONGUE OEDEMA ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
TYPE 2 DIABETES MELLITUS ( 4 FDA reports)
VAGINAL HAEMORRHAGE ( 4 FDA reports)
VITREOUS OPACITIES ( 4 FDA reports)
ABDOMINAL NEOPLASM ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
ANGIONEUROTIC OEDEMA ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
BLADDER DISORDER ( 3 FDA reports)
BLINDNESS UNILATERAL ( 3 FDA reports)
BLOOD AMYLASE INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 3 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 3 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 3 FDA reports)
BRAIN STEM HAEMORRHAGE ( 3 FDA reports)
BREAST CANCER FEMALE ( 3 FDA reports)
BREAST CANCER METASTATIC ( 3 FDA reports)
BREAST HAEMORRHAGE ( 3 FDA reports)
BURSITIS ( 3 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 3 FDA reports)
CATARACT OPERATION ( 3 FDA reports)
CHAPPED LIPS ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DECREASED VIBRATORY SENSE ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DENGUE FEVER ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
ECONOMIC PROBLEM ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
ENCEPHALITIS HERPES ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 3 FDA reports)
EXPIRED DRUG ADMINISTERED ( 3 FDA reports)
EYE IRRITATION ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
FEELING OF DESPAIR ( 3 FDA reports)
FIBROSIS ( 3 FDA reports)
FORMICATION ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GASTROINTESTINAL CARCINOMA ( 3 FDA reports)
GASTROINTESTINAL INFECTION ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
HIP FRACTURE ( 3 FDA reports)
HUNGER ( 3 FDA reports)
HYPERTENSIVE EMERGENCY ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOCHLORAEMIA ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
KIDNEY INFECTION ( 3 FDA reports)
LABYRINTHITIS ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 3 FDA reports)
LIMB INJURY ( 3 FDA reports)
LIP DRY ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
MENSTRUAL DISORDER ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
METABOLIC SYNDROME ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 3 FDA reports)
NECK MASS ( 3 FDA reports)
NEOPLASM RECURRENCE ( 3 FDA reports)
NO ADVERSE EVENT ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
ORAL PAIN ( 3 FDA reports)
ORGAN FAILURE ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
PANCREATITIS NECROTISING ( 3 FDA reports)
PELVIC PAIN ( 3 FDA reports)
PHOTOPHOBIA ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
POLYP ( 3 FDA reports)
PRESBYOPIA ( 3 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 3 FDA reports)
PROSTATIC DISORDER ( 3 FDA reports)
RECURRENT CANCER ( 3 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RETINAL DETACHMENT ( 3 FDA reports)
RETINAL DISORDER ( 3 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
RHEUMATOID FACTOR NEGATIVE ( 3 FDA reports)
SEXUAL DYSFUNCTION ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SJOGREN'S SYNDROME ( 3 FDA reports)
SKIN HYPERTROPHY ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
SURGERY ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
TRAUMATIC BRAIN INJURY ( 3 FDA reports)
TUMOUR INVASION ( 3 FDA reports)
ULCER ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 3 FDA reports)
UTERINE LEIOMYOMA ( 3 FDA reports)
VARICOSE VEIN ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
WRIST FRACTURE ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ABNORMAL WEIGHT GAIN ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ADHESION ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
APPETITE DISORDER ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
APPLICATION SITE INFLAMMATION ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
ARTERIAL BYPASS OPERATION ( 2 FDA reports)
ARTERIAL STENT INSERTION ( 2 FDA reports)
ARTHRITIS BACTERIAL ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
ARTHROSCOPY ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
BONE TRIMMING ( 2 FDA reports)
BREAST HYPERPLASIA ( 2 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CANDIDURIA ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 2 FDA reports)
CERVICAL DYSPLASIA ( 2 FDA reports)
CHONDROPATHY ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COMPRESSION FRACTURE ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORONARY ANGIOPLASTY ( 2 FDA reports)
CORONARY ARTERY BYPASS ( 2 FDA reports)
DERMAL CYST ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DEVICE MALFUNCTION ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DISABILITY ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DRUG-INDUCED LIVER INJURY ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
ESSENTIAL HYPERTENSION ( 2 FDA reports)
EYE LASER SURGERY ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GENITAL RASH ( 2 FDA reports)
GINGIVAL ULCERATION ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HAEMORRHAGIC ANAEMIA ( 2 FDA reports)
HAEMOSIDEROSIS ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HELICOBACTER TEST POSITIVE ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HERPES ZOSTER DISSEMINATED ( 2 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYPERALDOSTERONISM ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPERPLASIA ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
IIIRD NERVE PARALYSIS ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INJECTION SITE STINGING ( 2 FDA reports)
INTERCOSTAL NEURALGIA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTESTINAL POLYP ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LACRIMAL DISORDER ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LIGAMENT INJURY ( 2 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 2 FDA reports)
LIP HAEMORRHAGE ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LOSS OF EMPLOYMENT ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LYMPHOEDEMA ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MALIGNANT TUMOUR EXCISION ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MENINGISM ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MULTIMORBIDITY ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MYCETOMA MYCOTIC ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NEUROPATHIC ULCER ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 2 FDA reports)
OBESITY SURGERY ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OESOPHAGEAL DISORDER ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
OLIGOHYDRAMNIOS ( 2 FDA reports)
ONYCHOMYCOSIS ( 2 FDA reports)
ORAL INFECTION ( 2 FDA reports)
OSTEOCHONDROSIS ( 2 FDA reports)
OSTEOMYELITIS ACUTE ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
OVERWEIGHT ( 2 FDA reports)
PANNICULITIS ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PLASTIC SURGERY ( 2 FDA reports)
PLEURAL FIBROSIS ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
POST PROCEDURAL FISTULA ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PRIMARY SEQUESTRUM ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PRURITUS GENITAL ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RADIOTHERAPY ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 2 FDA reports)
REFRACTION DISORDER ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
RENAL PAIN ( 2 FDA reports)
RENAL SALT-WASTING SYNDROME ( 2 FDA reports)
RENAL VEIN OCCLUSION ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
RETINAL VEIN THROMBOSIS ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SEQUESTRECTOMY ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN TIGHTNESS ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
SLEEP TALKING ( 2 FDA reports)
SNORING ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
SPLENIC LESION ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SYSTOLIC DYSFUNCTION ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
TENDON INJURY ( 2 FDA reports)
TETANY ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
THYROIDITIS ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TONGUE DRY ( 2 FDA reports)
TONGUE HAEMORRHAGE ( 2 FDA reports)
TONGUE INJURY ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
TUMOUR ASSOCIATED FEVER ( 2 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 2 FDA reports)
ULCERATIVE KERATITIS ( 2 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
URETHRAL ATROPHY ( 2 FDA reports)
UTERINE DISORDER ( 2 FDA reports)
VASCULAR STENOSIS ( 2 FDA reports)
VASODILATION PROCEDURE ( 2 FDA reports)
VENOUS STENT INSERTION ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VERTEBRAL ARTERY THROMBOSIS ( 2 FDA reports)
VERTEBROPLASTY ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
VITREOUS DETACHMENT ( 2 FDA reports)
VULVAL CANCER ( 2 FDA reports)
WEIGHT LOSS POOR ( 2 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
YAWNING ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACROCHORDON ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADNEXA UTERI CYST ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL INFLAMMATION ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ATRIAL PRESSURE INCREASED ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AXILLARY NERVE INJURY ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIAL DNA TEST POSITIVE ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BACTERIAL TEST ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE DEBRIDEMENT ( 1 FDA reports)
BONE DENSITY ABNORMAL ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARCINOID TUMOUR OF THE SMALL BOWEL ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CATHETERISATION VENOUS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CORNEAL THICKENING ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
CRYPTORCHISM ( 1 FDA reports)
CSF CELL COUNT INCREASED ( 1 FDA reports)
CSF IMMUNOGLOBULIN INCREASED ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ELECTRONYSTAGMOGRAM ABNORMAL ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOETAL GROWTH RESTRICTION ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTRITIS BACTERIAL ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GINGIVAL INFECTION ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPNOTHERAPY ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPLANT SITE FIBROSIS ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCISIONAL DRAINAGE ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LARYNX IRRITATION ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MASS ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTATIC GASTRIC CANCER ( 1 FDA reports)
METHYLMALONIC ACIDURIA ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL LESION EXCISION ( 1 FDA reports)
OESOPHAGEAL MASS ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PANNICULITIS LOBULAR ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PERITONEAL MESOTHELIOMA MALIGNANT ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PROTEIN URINE ABSENT ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
RADIATION NECROSIS ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
REHABILITATION THERAPY ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT OEDEMA ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL ARTERY THROMBOSIS ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINOBRONCHITIS ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SKELETON DYSPLASIA ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SKULL MALFORMATION ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SMEAR SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SPINAL CORD NEOPLASM ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
STENT MALFUNCTION ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TENONECTOMY ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
TENOSYNOVITIS STENOSANS ( 1 FDA reports)
TENSION ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TOBACCO POISONING ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TUMOUR EXCISION ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UPPER EXTREMITY MASS ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE POTASSIUM ABNORMAL ( 1 FDA reports)
URINE POTASSIUM DECREASED ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WALKING DISTANCE TEST ABNORMAL ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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