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

PAIN ( 257 FDA reports)
NAUSEA ( 206 FDA reports)
FALL ( 181 FDA reports)
VOMITING ( 166 FDA reports)
DYSPNOEA ( 161 FDA reports)
PAIN IN EXTREMITY ( 155 FDA reports)
BACK PAIN ( 149 FDA reports)
FATIGUE ( 149 FDA reports)
ASTHENIA ( 148 FDA reports)
DIZZINESS ( 131 FDA reports)
MALAISE ( 126 FDA reports)
ARTHRALGIA ( 117 FDA reports)
OEDEMA PERIPHERAL ( 113 FDA reports)
WEIGHT DECREASED ( 99 FDA reports)
DRUG INEFFECTIVE ( 97 FDA reports)
GAIT DISTURBANCE ( 97 FDA reports)
HEADACHE ( 94 FDA reports)
FEELING ABNORMAL ( 89 FDA reports)
PYREXIA ( 86 FDA reports)
DIARRHOEA ( 85 FDA reports)
CONSTIPATION ( 82 FDA reports)
ANXIETY ( 80 FDA reports)
DEPRESSION ( 76 FDA reports)
RENAL FAILURE ( 71 FDA reports)
PNEUMONIA ( 70 FDA reports)
ABDOMINAL PAIN ( 62 FDA reports)
DEATH ( 60 FDA reports)
CONFUSIONAL STATE ( 59 FDA reports)
HYPERTENSION ( 58 FDA reports)
INSOMNIA ( 57 FDA reports)
LOSS OF CONSCIOUSNESS ( 57 FDA reports)
TREMOR ( 57 FDA reports)
ABDOMINAL PAIN UPPER ( 56 FDA reports)
HYPOAESTHESIA ( 56 FDA reports)
INFLUENZA LIKE ILLNESS ( 56 FDA reports)
MOBILITY DECREASED ( 56 FDA reports)
WEIGHT INCREASED ( 56 FDA reports)
MUSCLE SPASMS ( 55 FDA reports)
BLOOD PRESSURE INCREASED ( 54 FDA reports)
MUSCULAR WEAKNESS ( 54 FDA reports)
BONE DISORDER ( 53 FDA reports)
DEHYDRATION ( 53 FDA reports)
VISION BLURRED ( 52 FDA reports)
ABASIA ( 51 FDA reports)
DECREASED APPETITE ( 51 FDA reports)
CHEST PAIN ( 50 FDA reports)
BLOOD GLUCOSE INCREASED ( 49 FDA reports)
BONE PAIN ( 48 FDA reports)
CEREBROVASCULAR ACCIDENT ( 47 FDA reports)
DRUG DOSE OMISSION ( 47 FDA reports)
CONTUSION ( 46 FDA reports)
SOMNOLENCE ( 44 FDA reports)
RASH ( 43 FDA reports)
CONDITION AGGRAVATED ( 42 FDA reports)
HYPOTENSION ( 42 FDA reports)
COUGH ( 41 FDA reports)
HYPERHIDROSIS ( 41 FDA reports)
ANAEMIA ( 40 FDA reports)
PULMONARY EMBOLISM ( 40 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 39 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 38 FDA reports)
INJURY ( 38 FDA reports)
MYALGIA ( 38 FDA reports)
NECK PAIN ( 38 FDA reports)
URINARY TRACT INFECTION ( 38 FDA reports)
DEEP VEIN THROMBOSIS ( 37 FDA reports)
HIP FRACTURE ( 37 FDA reports)
MUSCULOSKELETAL PAIN ( 37 FDA reports)
PAIN IN JAW ( 37 FDA reports)
PARAESTHESIA ( 37 FDA reports)
AMNESIA ( 35 FDA reports)
JOINT SWELLING ( 35 FDA reports)
HYPOPHAGIA ( 34 FDA reports)
PRURITUS ( 34 FDA reports)
AGGRESSION ( 33 FDA reports)
BALANCE DISORDER ( 33 FDA reports)
HAEMORRHAGE ( 33 FDA reports)
MYOCARDIAL INFARCTION ( 33 FDA reports)
ARTHROPATHY ( 32 FDA reports)
HYPERSENSITIVITY ( 32 FDA reports)
INJECTION SITE PAIN ( 32 FDA reports)
ABDOMINAL DISCOMFORT ( 31 FDA reports)
ERYTHEMA ( 31 FDA reports)
INJECTION SITE HAEMATOMA ( 31 FDA reports)
ARTHRITIS ( 30 FDA reports)
DRUG INTERACTION ( 30 FDA reports)
HAEMOGLOBIN DECREASED ( 30 FDA reports)
HOSPITALISATION ( 30 FDA reports)
IMPAIRED HEALING ( 30 FDA reports)
TOOTH EXTRACTION ( 30 FDA reports)
CONVULSION ( 29 FDA reports)
INFLAMMATION ( 29 FDA reports)
MEMORY IMPAIRMENT ( 29 FDA reports)
OVERDOSE ( 29 FDA reports)
PLATELET COUNT DECREASED ( 29 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 28 FDA reports)
EMOTIONAL DISTRESS ( 28 FDA reports)
HEPATIC ENZYME INCREASED ( 28 FDA reports)
CARDIAC DISORDER ( 27 FDA reports)
HEAD INJURY ( 27 FDA reports)
INFECTION ( 27 FDA reports)
OSTEONECROSIS ( 27 FDA reports)
PANCREATITIS ( 27 FDA reports)
ATRIAL FIBRILLATION ( 26 FDA reports)
HALLUCINATION ( 26 FDA reports)
RENAL IMPAIRMENT ( 26 FDA reports)
SURGERY ( 26 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 25 FDA reports)
CARDIAC ARREST ( 25 FDA reports)
OFF LABEL USE ( 25 FDA reports)
OSTEOMYELITIS ( 25 FDA reports)
RESPIRATORY FAILURE ( 25 FDA reports)
VERTIGO ( 25 FDA reports)
BONE DENSITY DECREASED ( 24 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 24 FDA reports)
DIABETES MELLITUS ( 24 FDA reports)
DISORIENTATION ( 24 FDA reports)
DRY MOUTH ( 24 FDA reports)
FEAR ( 24 FDA reports)
JAUNDICE ( 24 FDA reports)
NEUROPATHY PERIPHERAL ( 24 FDA reports)
ROAD TRAFFIC ACCIDENT ( 24 FDA reports)
SPINAL FRACTURE ( 24 FDA reports)
STRESS ( 24 FDA reports)
VISUAL IMPAIRMENT ( 24 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 23 FDA reports)
BACK DISORDER ( 23 FDA reports)
LUNG INFILTRATION ( 23 FDA reports)
MIGRAINE ( 23 FDA reports)
OSTEOARTHRITIS ( 23 FDA reports)
PALPITATIONS ( 23 FDA reports)
VISUAL ACUITY REDUCED ( 23 FDA reports)
CHOLELITHIASIS ( 22 FDA reports)
MEDICATION ERROR ( 22 FDA reports)
NEOPLASM MALIGNANT ( 22 FDA reports)
THROMBOCYTOPENIA ( 22 FDA reports)
ABDOMINAL DISTENSION ( 21 FDA reports)
DISCOMFORT ( 21 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 21 FDA reports)
LETHARGY ( 21 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 21 FDA reports)
NASOPHARYNGITIS ( 21 FDA reports)
SKIN DISORDER ( 21 FDA reports)
SKIN INDURATION ( 21 FDA reports)
THROMBOSIS ( 21 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 21 FDA reports)
BLOOD CALCIUM DECREASED ( 20 FDA reports)
BLOOD CREATININE INCREASED ( 20 FDA reports)
FIBROSIS ( 20 FDA reports)
GASTROINTESTINAL DISORDER ( 20 FDA reports)
HEPATITIS ( 20 FDA reports)
RENAL FAILURE ACUTE ( 20 FDA reports)
RESPIRATORY ARREST ( 20 FDA reports)
RHEUMATOID ARTHRITIS ( 20 FDA reports)
RIB FRACTURE ( 20 FDA reports)
SKIN DISCOLOURATION ( 20 FDA reports)
SYNCOPE ( 20 FDA reports)
ABNORMAL DREAMS ( 19 FDA reports)
ABSCESS ORAL ( 19 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 19 FDA reports)
CARDIAC FAILURE ( 19 FDA reports)
DEFORMITY ( 19 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 19 FDA reports)
EPISTAXIS ( 19 FDA reports)
FRACTURE NONUNION ( 19 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 19 FDA reports)
HOMICIDAL IDEATION ( 19 FDA reports)
JOINT INJURY ( 19 FDA reports)
MULTI-ORGAN FAILURE ( 19 FDA reports)
SEPSIS ( 19 FDA reports)
ANKLE FRACTURE ( 18 FDA reports)
ATELECTASIS ( 18 FDA reports)
CHOLECYSTITIS CHRONIC ( 18 FDA reports)
DEPRESSED MOOD ( 18 FDA reports)
DYSSTASIA ( 18 FDA reports)
GALLBLADDER DISORDER ( 18 FDA reports)
PLEURAL EFFUSION ( 18 FDA reports)
RASH MACULAR ( 18 FDA reports)
TENDERNESS ( 18 FDA reports)
UNEVALUABLE EVENT ( 18 FDA reports)
ARTERIOSCLEROSIS ( 17 FDA reports)
BLOOD UREA INCREASED ( 17 FDA reports)
CYST ( 17 FDA reports)
HAEMATOCRIT DECREASED ( 17 FDA reports)
HEART RATE INCREASED ( 17 FDA reports)
LIMB INJURY ( 17 FDA reports)
MENTAL STATUS CHANGES ( 17 FDA reports)
PROTHROMBIN TIME PROLONGED ( 17 FDA reports)
PULMONARY MASS ( 17 FDA reports)
SCAR ( 17 FDA reports)
SPINAL DISORDER ( 17 FDA reports)
SUICIDAL IDEATION ( 17 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 17 FDA reports)
DISEASE PROGRESSION ( 16 FDA reports)
DYSPHAGIA ( 16 FDA reports)
INTESTINAL ULCER ( 16 FDA reports)
MOVEMENT DISORDER ( 16 FDA reports)
OROPHARYNGEAL PAIN ( 16 FDA reports)
OSTEOPENIA ( 16 FDA reports)
PELVIC FRACTURE ( 16 FDA reports)
ROTATOR CUFF SYNDROME ( 16 FDA reports)
SQUAMOUS CELL CARCINOMA ( 16 FDA reports)
UPPER LIMB FRACTURE ( 16 FDA reports)
ANHEDONIA ( 15 FDA reports)
AORTIC STENOSIS ( 15 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 15 FDA reports)
DRUG DEPENDENCE ( 15 FDA reports)
FOOT FRACTURE ( 15 FDA reports)
HEART RATE DECREASED ( 15 FDA reports)
IRRITABILITY ( 15 FDA reports)
NON-SMALL CELL LUNG CANCER ( 15 FDA reports)
SPEECH DISORDER ( 15 FDA reports)
SWELLING FACE ( 15 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 15 FDA reports)
UNRESPONSIVE TO STIMULI ( 15 FDA reports)
BIOPSY BONE ABNORMAL ( 14 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 14 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 14 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 14 FDA reports)
CHILLS ( 14 FDA reports)
COLONOSCOPY ABNORMAL ( 14 FDA reports)
DISTURBANCE IN ATTENTION ( 14 FDA reports)
DYSPEPSIA ( 14 FDA reports)
FLATULENCE ( 14 FDA reports)
HAEMORRHAGIC DIATHESIS ( 14 FDA reports)
HEPATIC STEATOSIS ( 14 FDA reports)
HERPES ZOSTER ( 14 FDA reports)
HIP ARTHROPLASTY ( 14 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 14 FDA reports)
INCORRECT DOSE ADMINISTERED ( 14 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 14 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 14 FDA reports)
INTESTINAL MASS ( 14 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 14 FDA reports)
NEOPLASM PROGRESSION ( 14 FDA reports)
NERVOUSNESS ( 14 FDA reports)
ORAL NEOPLASM BENIGN ( 14 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 14 FDA reports)
SCAN ABNORMAL ( 14 FDA reports)
SWELLING ( 14 FDA reports)
TACHYCARDIA ( 14 FDA reports)
X-RAY ABNORMAL ( 14 FDA reports)
ANOREXIA ( 13 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 13 FDA reports)
DYSARTHRIA ( 13 FDA reports)
DYSGEUSIA ( 13 FDA reports)
FIBROMYALGIA ( 13 FDA reports)
HYPOCALCAEMIA ( 13 FDA reports)
ILL-DEFINED DISORDER ( 13 FDA reports)
LIMB DISCOMFORT ( 13 FDA reports)
LOWER LIMB FRACTURE ( 13 FDA reports)
MENTAL DISORDER ( 13 FDA reports)
NEURALGIA ( 13 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 13 FDA reports)
OSTEONECROSIS OF JAW ( 13 FDA reports)
SEPTIC SHOCK ( 13 FDA reports)
SPINAL COLUMN STENOSIS ( 13 FDA reports)
TRANSFUSION ( 13 FDA reports)
BLOOD GLUCOSE DECREASED ( 12 FDA reports)
BLOOD PRESSURE DECREASED ( 12 FDA reports)
CEREBRAL HAEMORRHAGE ( 12 FDA reports)
CHOLECYSTECTOMY ( 12 FDA reports)
CHROMATURIA ( 12 FDA reports)
EUPHORIC MOOD ( 12 FDA reports)
EXOSTOSIS ( 12 FDA reports)
HAEMATURIA ( 12 FDA reports)
HAEMOPTYSIS ( 12 FDA reports)
HEPATOTOXICITY ( 12 FDA reports)
HYPOXIA ( 12 FDA reports)
INFLUENZA ( 12 FDA reports)
INTENTIONAL DRUG MISUSE ( 12 FDA reports)
JAW DISORDER ( 12 FDA reports)
MYOPIA ( 12 FDA reports)
ORAL SURGERY ( 12 FDA reports)
SKIN TIGHTNESS ( 12 FDA reports)
UNDERDOSE ( 12 FDA reports)
BLISTER ( 11 FDA reports)
BLOOD POTASSIUM DECREASED ( 11 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 11 FDA reports)
BONE OPERATION ( 11 FDA reports)
BURNING SENSATION ( 11 FDA reports)
CELLULITIS ( 11 FDA reports)
EMPHYSEMA ( 11 FDA reports)
ENDOTRACHEAL INTUBATION ( 11 FDA reports)
FACE INJURY ( 11 FDA reports)
FISTULA ( 11 FDA reports)
FLUID RETENTION ( 11 FDA reports)
HIATUS HERNIA ( 11 FDA reports)
HYPOKALAEMIA ( 11 FDA reports)
LEUKOCYTOSIS ( 11 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 11 FDA reports)
OBESITY ( 11 FDA reports)
PRESYNCOPE ( 11 FDA reports)
RENAL INJURY ( 11 FDA reports)
SKIN EXFOLIATION ( 11 FDA reports)
SLEEP DISORDER ( 11 FDA reports)
TOOTH LOSS ( 11 FDA reports)
URTICARIA ( 11 FDA reports)
ACNE ( 10 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 10 FDA reports)
AMMONIA INCREASED ( 10 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 10 FDA reports)
BLOOD POTASSIUM INCREASED ( 10 FDA reports)
BLOOD SODIUM DECREASED ( 10 FDA reports)
CARDIO-RESPIRATORY ARREST ( 10 FDA reports)
CARDIOMYOPATHY ( 10 FDA reports)
COGNITIVE DISORDER ( 10 FDA reports)
COMA ( 10 FDA reports)
DIPLOPIA ( 10 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 10 FDA reports)
DYSURIA ( 10 FDA reports)
HYPOGLYCAEMIA ( 10 FDA reports)
INJECTION SITE ERYTHEMA ( 10 FDA reports)
KNEE ARTHROPLASTY ( 10 FDA reports)
MUSCLE TIGHTNESS ( 10 FDA reports)
NEPHROLITHIASIS ( 10 FDA reports)
ORAL CANDIDIASIS ( 10 FDA reports)
POLLAKIURIA ( 10 FDA reports)
PRODUCT QUALITY ISSUE ( 10 FDA reports)
PULMONARY HYPERTENSION ( 10 FDA reports)
RENAL DISORDER ( 10 FDA reports)
RENAL PAIN ( 10 FDA reports)
RHABDOMYOLYSIS ( 10 FDA reports)
SINUSITIS ( 10 FDA reports)
SKIN LESION ( 10 FDA reports)
SPINAL COMPRESSION FRACTURE ( 10 FDA reports)
SUICIDE ATTEMPT ( 10 FDA reports)
SWOLLEN TONGUE ( 10 FDA reports)
THINKING ABNORMAL ( 10 FDA reports)
TINNITUS ( 10 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 10 FDA reports)
ACCIDENTAL OVERDOSE ( 9 FDA reports)
ALOPECIA ( 9 FDA reports)
BACTERIAL TEST POSITIVE ( 9 FDA reports)
BEDRIDDEN ( 9 FDA reports)
BLOOD BILIRUBIN INCREASED ( 9 FDA reports)
BLOOD CALCIUM INCREASED ( 9 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 9 FDA reports)
CARDIOMEGALY ( 9 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 9 FDA reports)
CORONARY ARTERY DISEASE ( 9 FDA reports)
CRYING ( 9 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 9 FDA reports)
FEELING HOT ( 9 FDA reports)
FEMUR FRACTURE ( 9 FDA reports)
GASTRITIS ( 9 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 9 FDA reports)
HIP SURGERY ( 9 FDA reports)
HOT FLUSH ( 9 FDA reports)
IMPAIRED DRIVING ABILITY ( 9 FDA reports)
LIP SWELLING ( 9 FDA reports)
LIVER DISORDER ( 9 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 9 FDA reports)
LOCAL SWELLING ( 9 FDA reports)
MENTAL IMPAIRMENT ( 9 FDA reports)
MOTOR DYSFUNCTION ( 9 FDA reports)
MULTIPLE SCLEROSIS ( 9 FDA reports)
OSTEITIS ( 9 FDA reports)
PRURITUS GENERALISED ( 9 FDA reports)
PULMONARY OEDEMA ( 9 FDA reports)
RASH PRURITIC ( 9 FDA reports)
RESPIRATORY DISTRESS ( 9 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 9 FDA reports)
SEDATION ( 9 FDA reports)
SENSORY LOSS ( 9 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 9 FDA reports)
URINARY INCONTINENCE ( 9 FDA reports)
URINE OUTPUT DECREASED ( 9 FDA reports)
ABSCESS ( 8 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 8 FDA reports)
ADVERSE DRUG REACTION ( 8 FDA reports)
BLINDNESS UNILATERAL ( 8 FDA reports)
BLOOD URINE PRESENT ( 8 FDA reports)
BODY HEIGHT DECREASED ( 8 FDA reports)
CATARACT ( 8 FDA reports)
CHOLECYSTITIS ( 8 FDA reports)
DEBRIDEMENT ( 8 FDA reports)
DRY SKIN ( 8 FDA reports)
FLUSHING ( 8 FDA reports)
GASTRIC DISORDER ( 8 FDA reports)
GRAND MAL CONVULSION ( 8 FDA reports)
HAEMATOMA ( 8 FDA reports)
HYPERKALAEMIA ( 8 FDA reports)
HYPERTHERMIA ( 8 FDA reports)
JOINT STIFFNESS ( 8 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 8 FDA reports)
LUNG DISORDER ( 8 FDA reports)
METASTASES TO LIVER ( 8 FDA reports)
OCULAR ICTERUS ( 8 FDA reports)
OEDEMA ( 8 FDA reports)
PAROTID GLAND ENLARGEMENT ( 8 FDA reports)
PERICARDIAL EFFUSION ( 8 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 8 FDA reports)
PROCEDURAL PAIN ( 8 FDA reports)
RASH PAPULAR ( 8 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 8 FDA reports)
RESPIRATORY DISORDER ( 8 FDA reports)
RHINORRHOEA ( 8 FDA reports)
SKIN BURNING SENSATION ( 8 FDA reports)
SKIN FIBROSIS ( 8 FDA reports)
SKIN HYPERTROPHY ( 8 FDA reports)
SPONDYLITIS ( 8 FDA reports)
STOMACH DISCOMFORT ( 8 FDA reports)
WITHDRAWAL SYNDROME ( 8 FDA reports)
AGITATION ( 7 FDA reports)
ANAPHYLACTIC REACTION ( 7 FDA reports)
AREFLEXIA ( 7 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 7 FDA reports)
BLOOD ALBUMIN DECREASED ( 7 FDA reports)
BLOOD TEST ABNORMAL ( 7 FDA reports)
BREAST PAIN ( 7 FDA reports)
CAROTID BRUIT ( 7 FDA reports)
CHEST DISCOMFORT ( 7 FDA reports)
CHOLECYSTITIS ACUTE ( 7 FDA reports)
CORONARY ARTERY OCCLUSION ( 7 FDA reports)
DILATATION VENTRICULAR ( 7 FDA reports)
EYE SWELLING ( 7 FDA reports)
FACIAL PAIN ( 7 FDA reports)
FEBRILE NEUTROPENIA ( 7 FDA reports)
GALLBLADDER OPERATION ( 7 FDA reports)
GASTRIC HAEMORRHAGE ( 7 FDA reports)
GASTROENTERITIS ( 7 FDA reports)
GOUT ( 7 FDA reports)
HEART RATE IRREGULAR ( 7 FDA reports)
HYPERGLYCAEMIA ( 7 FDA reports)
HYPERSOMNIA ( 7 FDA reports)
IMPAIRED WORK ABILITY ( 7 FDA reports)
INJECTION SITE ULCER ( 7 FDA reports)
INTENTIONAL OVERDOSE ( 7 FDA reports)
IRON DEFICIENCY ANAEMIA ( 7 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 7 FDA reports)
MEDICAL DEVICE COMPLICATION ( 7 FDA reports)
METASTASES TO BONE ( 7 FDA reports)
MULTIPLE MYELOMA ( 7 FDA reports)
MUSCLE STRAIN ( 7 FDA reports)
NERVOUS SYSTEM DISORDER ( 7 FDA reports)
NEUTROPENIA ( 7 FDA reports)
OSTEOPOROSIS ( 7 FDA reports)
PALLOR ( 7 FDA reports)
PANCREATIC CARCINOMA ( 7 FDA reports)
PANIC ATTACK ( 7 FDA reports)
PRESBYOPIA ( 7 FDA reports)
PULMONARY FIBROSIS ( 7 FDA reports)
RASH ERYTHEMATOUS ( 7 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 7 FDA reports)
SCIATICA ( 7 FDA reports)
SCOLIOSIS ( 7 FDA reports)
SPINAL FUSION SURGERY ( 7 FDA reports)
SPLENOMEGALY ( 7 FDA reports)
SPONDYLOLISTHESIS ( 7 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 7 FDA reports)
TRANSAMINASES INCREASED ( 7 FDA reports)
ANURIA ( 6 FDA reports)
APATHY ( 6 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
ASCITES ( 6 FDA reports)
BILIARY DYSKINESIA ( 6 FDA reports)
BLOOD COUNT ABNORMAL ( 6 FDA reports)
BRADYCARDIA ( 6 FDA reports)
CALCIUM DEFICIENCY ( 6 FDA reports)
CANDIDIASIS ( 6 FDA reports)
CARDIAC PACEMAKER INSERTION ( 6 FDA reports)
CARPAL TUNNEL SYNDROME ( 6 FDA reports)
COLD SWEAT ( 6 FDA reports)
COORDINATION ABNORMAL ( 6 FDA reports)
DELIRIUM ( 6 FDA reports)
DISABILITY ( 6 FDA reports)
DIVERTICULITIS ( 6 FDA reports)
DRUG ABUSE ( 6 FDA reports)
DRUG ADMINISTRATION ERROR ( 6 FDA reports)
EXERCISE TOLERANCE DECREASED ( 6 FDA reports)
EYE DISORDER ( 6 FDA reports)
EYE PAIN ( 6 FDA reports)
FAECAL INCONTINENCE ( 6 FDA reports)
GASTROENTERITIS VIRAL ( 6 FDA reports)
GINGIVAL EROSION ( 6 FDA reports)
HAND FRACTURE ( 6 FDA reports)
HEPATIC FAILURE ( 6 FDA reports)
HYPERKERATOSIS ( 6 FDA reports)
HYPOKINESIA ( 6 FDA reports)
INCONTINENCE ( 6 FDA reports)
LACRIMATION INCREASED ( 6 FDA reports)
LARGE INTESTINE PERFORATION ( 6 FDA reports)
LEUKOPENIA ( 6 FDA reports)
LUDWIG ANGINA ( 6 FDA reports)
LYME DISEASE ( 6 FDA reports)
LYMPHADENOPATHY ( 6 FDA reports)
MAJOR DEPRESSION ( 6 FDA reports)
MASS ( 6 FDA reports)
MASTICATION DISORDER ( 6 FDA reports)
MELAENA ( 6 FDA reports)
METASTATIC NEOPLASM ( 6 FDA reports)
MOOD SWINGS ( 6 FDA reports)
MUSCLE INJURY ( 6 FDA reports)
NEOPLASM ( 6 FDA reports)
NERVE COMPRESSION ( 6 FDA reports)
OXYGEN SATURATION DECREASED ( 6 FDA reports)
PANCREATIC DISORDER ( 6 FDA reports)
PANCREATIC INJURY ( 6 FDA reports)
PANCREATITIS ACUTE ( 6 FDA reports)
PARANOIA ( 6 FDA reports)
PERIARTHRITIS ( 6 FDA reports)
PRECANCEROUS MUCOSAL LESION ( 6 FDA reports)
PROSTATE CANCER ( 6 FDA reports)
PULMONARY INFARCTION ( 6 FDA reports)
RENAL CELL CARCINOMA ( 6 FDA reports)
RESPIRATORY RATE DECREASED ( 6 FDA reports)
RETCHING ( 6 FDA reports)
SICK SINUS SYNDROME ( 6 FDA reports)
SINUS TACHYCARDIA ( 6 FDA reports)
SKIN PLAQUE ( 6 FDA reports)
SPINAL OPERATION ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 6 FDA reports)
STOMATITIS ( 6 FDA reports)
SWEAT GLAND DISORDER ( 6 FDA reports)
TREATMENT NONCOMPLIANCE ( 6 FDA reports)
VASODILATATION ( 6 FDA reports)
VENOUS INSUFFICIENCY ( 6 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 6 FDA reports)
VISUAL DISTURBANCE ( 6 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 6 FDA reports)
WOUND ( 6 FDA reports)
ABDOMINAL HERNIA ( 5 FDA reports)
ACUTE PULMONARY OEDEMA ( 5 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
ANGER ( 5 FDA reports)
APHAGIA ( 5 FDA reports)
APHASIA ( 5 FDA reports)
APPLICATION SITE IRRITATION ( 5 FDA reports)
APPLICATION SITE PAIN ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 5 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 5 FDA reports)
BLOOD BICARBONATE DECREASED ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
BRONCHOPNEUMONIA ( 5 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 5 FDA reports)
CARDIOVASCULAR DISORDER ( 5 FDA reports)
CATHETERISATION CARDIAC ( 5 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 5 FDA reports)
COLITIS ( 5 FDA reports)
COLITIS ULCERATIVE ( 5 FDA reports)
COMPLETED SUICIDE ( 5 FDA reports)
DECREASED ACTIVITY ( 5 FDA reports)
DERMATITIS ( 5 FDA reports)
DEVICE RELATED INFECTION ( 5 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 5 FDA reports)
DRUG HYPERSENSITIVITY ( 5 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 5 FDA reports)
ECZEMA ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 5 FDA reports)
ENDOCRINE DISORDER ( 5 FDA reports)
EPILEPSY ( 5 FDA reports)
GALLBLADDER INJURY ( 5 FDA reports)
GASTRIC CANCER ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
GINGIVAL SWELLING ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HEARING IMPAIRED ( 5 FDA reports)
HYPONATRAEMIA ( 5 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 5 FDA reports)
INDURATION ( 5 FDA reports)
INJECTION SITE HAEMORRHAGE ( 5 FDA reports)
INJECTION SITE NODULE ( 5 FDA reports)
INJECTION SITE RASH ( 5 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 5 FDA reports)
LIGAMENT SPRAIN ( 5 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
LUNG NEOPLASM ( 5 FDA reports)
MENINGIOMA ( 5 FDA reports)
METASTASES TO PLEURA ( 5 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 5 FDA reports)
MYOCARDIAL ISCHAEMIA ( 5 FDA reports)
NERVE INJURY ( 5 FDA reports)
OCULAR HYPERAEMIA ( 5 FDA reports)
ORAL PAIN ( 5 FDA reports)
ORTHOSIS USER ( 5 FDA reports)
OVARIAN CANCER ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
PELVIC PAIN ( 5 FDA reports)
PLATELET COUNT ABNORMAL ( 5 FDA reports)
POISONING ( 5 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 5 FDA reports)
PRODUCTIVE COUGH ( 5 FDA reports)
PURPURA ( 5 FDA reports)
RASH PUSTULAR ( 5 FDA reports)
RETINAL HAEMORRHAGE ( 5 FDA reports)
SENSATION OF HEAVINESS ( 5 FDA reports)
SENSORY DISTURBANCE ( 5 FDA reports)
SERUM FERRITIN INCREASED ( 5 FDA reports)
SHOCK ( 5 FDA reports)
SKIN INJURY ( 5 FDA reports)
SPINAL LAMINECTOMY ( 5 FDA reports)
THERMAL BURN ( 5 FDA reports)
TYPE 1 DIABETES MELLITUS ( 5 FDA reports)
ULCER ( 5 FDA reports)
URINARY RETENTION ( 5 FDA reports)
URINE ANALYSIS ABNORMAL ( 5 FDA reports)
VENTRICULAR HYPOKINESIA ( 5 FDA reports)
VITAMIN A DEFICIENCY ( 5 FDA reports)
ACIDOSIS ( 4 FDA reports)
AKATHISIA ( 4 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
ANGIOGRAM ( 4 FDA reports)
APPENDICITIS PERFORATED ( 4 FDA reports)
APPLICATION SITE RASH ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
BACK INJURY ( 4 FDA reports)
BILIARY COLIC ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 4 FDA reports)
BLOOD DISORDER ( 4 FDA reports)
BLOOD PRESSURE ABNORMAL ( 4 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 4 FDA reports)
BLOOD URIC ACID INCREASED ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
BREAST CANCER METASTATIC ( 4 FDA reports)
BURSITIS ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
CAROTID ARTERY OCCLUSION ( 4 FDA reports)
CATATONIA ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
COMMUNICATION DISORDER ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
CYSTITIS ( 4 FDA reports)
DEAFNESS ( 4 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 4 FDA reports)
DEVICE BREAKAGE ( 4 FDA reports)
DEVICE FAILURE ( 4 FDA reports)
DEVICE OCCLUSION ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DILATATION ATRIAL ( 4 FDA reports)
DIVERTICULUM INTESTINAL ( 4 FDA reports)
DRUG PRESCRIBING ERROR ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
EATING DISORDER ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 4 FDA reports)
ENERGY INCREASED ( 4 FDA reports)
ERYTHEMA NODOSUM LEPROSUM ( 4 FDA reports)
ESCHAR ( 4 FDA reports)
EXCORIATION ( 4 FDA reports)
EXPOSED BONE IN JAW ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
FAECALOMA ( 4 FDA reports)
FAECES DISCOLOURED ( 4 FDA reports)
FEAR OF FALLING ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
FLUID INTAKE REDUCED ( 4 FDA reports)
FRACTURE ( 4 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 4 FDA reports)
FRUSTRATION ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
GINGIVAL PAIN ( 4 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 4 FDA reports)
HAEMORRHOIDS ( 4 FDA reports)
HYDROCEPHALUS ( 4 FDA reports)
HYPERTENSIVE CRISIS ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
ILEUS ( 4 FDA reports)
INADEQUATE ANALGESIA ( 4 FDA reports)
INCREASED APPETITE ( 4 FDA reports)
INCREASED TENDENCY TO BRUISE ( 4 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 4 FDA reports)
IRRITABLE BOWEL SYNDROME ( 4 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 4 FDA reports)
JOINT ARTHROPLASTY ( 4 FDA reports)
JOINT EFFUSION ( 4 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
LYMPHOEDEMA ( 4 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 4 FDA reports)
METASTASES TO LYMPH NODES ( 4 FDA reports)
MONOPARESIS ( 4 FDA reports)
MOOD ALTERED ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE ( 4 FDA reports)
MUSCLE DISORDER ( 4 FDA reports)
MUSCULOSKELETAL DISORDER ( 4 FDA reports)
NECK INJURY ( 4 FDA reports)
NEPHROSCLEROSIS ( 4 FDA reports)
NIGHT SWEATS ( 4 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 4 FDA reports)
PANIC REACTION ( 4 FDA reports)
PARALYSIS ( 4 FDA reports)
PARAPLEGIA ( 4 FDA reports)
PERICARDITIS ( 4 FDA reports)
PERIORBITAL HAEMATOMA ( 4 FDA reports)
PERIOSTITIS HYPERTROPHIC ( 4 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
PETIT MAL EPILEPSY ( 4 FDA reports)
PHLEBITIS ( 4 FDA reports)
PLEURISY ( 4 FDA reports)
PLEURITIC PAIN ( 4 FDA reports)
PNEUMATOSIS INTESTINALIS ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 4 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 4 FDA reports)
PRIMARY SEQUESTRUM ( 4 FDA reports)
PSORIASIS ( 4 FDA reports)
PYURIA ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
RESUSCITATION ( 4 FDA reports)
SKELETAL INJURY ( 4 FDA reports)
SKIN CANCER ( 4 FDA reports)
SKIN FISSURES ( 4 FDA reports)
SKIN LACERATION ( 4 FDA reports)
SKIN NODULE ( 4 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 4 FDA reports)
SPINAL DEFORMITY ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
TENDON RUPTURE ( 4 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 4 FDA reports)
THROMBOPHLEBITIS ( 4 FDA reports)
TOOTH DISORDER ( 4 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 4 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 4 FDA reports)
TRIGGER FINGER ( 4 FDA reports)
TUMOUR LYSIS SYNDROME ( 4 FDA reports)
URINARY HESITATION ( 4 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 4 FDA reports)
VENA CAVA THROMBOSIS ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ABNORMAL CLOTTING FACTOR ( 3 FDA reports)
ABORTION INDUCED ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 3 FDA reports)
ADHESION ( 3 FDA reports)
ALCOHOL INDUCED PERSISTING DEMENTIA ( 3 FDA reports)
ALCOHOL INTOLERANCE ( 3 FDA reports)
ALCOHOL USE ( 3 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
APPLICATION SITE BURN ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
APPLICATION SITE REACTION ( 3 FDA reports)
APPLICATION SITE VESICLES ( 3 FDA reports)
ARTERIAL STENOSIS ( 3 FDA reports)
ARTHRODESIS ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
BABESIOSIS ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 3 FDA reports)
BENIGN NEOPLASM ( 3 FDA reports)
BILE DUCT OBSTRUCTION ( 3 FDA reports)
BILE DUCT STONE ( 3 FDA reports)
BILIARY DILATATION ( 3 FDA reports)
BLADDER DISORDER ( 3 FDA reports)
BLADDER DYSFUNCTION ( 3 FDA reports)
BLOOD LACTIC ACID INCREASED ( 3 FDA reports)
BLOOD UREA ABNORMAL ( 3 FDA reports)
BRADYPHRENIA ( 3 FDA reports)
BRAIN INJURY ( 3 FDA reports)
BREAST CANCER RECURRENT ( 3 FDA reports)
CARDIAC VALVE DISEASE ( 3 FDA reports)
CAUDA EQUINA SYNDROME ( 3 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 3 FDA reports)
CERVICAL MYELOPATHY ( 3 FDA reports)
CHANGE OF BOWEL HABIT ( 3 FDA reports)
CHONDROPATHY ( 3 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 3 FDA reports)
COMPRESSION FRACTURE ( 3 FDA reports)
CONCUSSION ( 3 FDA reports)
CRYSTAL URINE PRESENT ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DEMYELINATION ( 3 FDA reports)
DEPENDENCE ( 3 FDA reports)
DEVICE DISLOCATION ( 3 FDA reports)
DEVICE MALFUNCTION ( 3 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
DROOLING ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
DRUG RESISTANCE ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
DUODENITIS ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
EAR DISORDER ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
ENDODONTIC PROCEDURE ( 3 FDA reports)
ENTEROCOCCAL INFECTION ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
ESCHERICHIA INFECTION ( 3 FDA reports)
EXPIRED DRUG ADMINISTERED ( 3 FDA reports)
FEEDING DISORDER ( 3 FDA reports)
FEMORAL NECK FRACTURE ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
FOOT DEFORMITY ( 3 FDA reports)
FORMICATION ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HAEMATOCRIT ( 3 FDA reports)
HAEMOGLOBIN ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
HAIR GROWTH ABNORMAL ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEPATITIS B ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
HUMERUS FRACTURE ( 3 FDA reports)
HYPERAESTHESIA ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPOACUSIS ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
IMMOBILE ( 3 FDA reports)
IMPULSE-CONTROL DISORDER ( 3 FDA reports)
INAPPROPRIATE AFFECT ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
INJECTION SITE EXTRAVASATION ( 3 FDA reports)
INJECTION SITE INFECTION ( 3 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 3 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 3 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 3 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 3 FDA reports)
JOINT CONTRACTURE ( 3 FDA reports)
JOINT DISLOCATION ( 3 FDA reports)
JOINT SPRAIN ( 3 FDA reports)
KIDNEY INFECTION ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LACERATION ( 3 FDA reports)
LIBIDO DECREASED ( 3 FDA reports)
LIMB DEFORMITY ( 3 FDA reports)
LIVER INJURY ( 3 FDA reports)
LOOSE TOOTH ( 3 FDA reports)
LUPUS-LIKE SYNDROME ( 3 FDA reports)
LYMPHOCYTE COUNT ( 3 FDA reports)
MECHANICAL VENTILATION ( 3 FDA reports)
MENINGITIS ( 3 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
METASTASES TO MENINGES ( 3 FDA reports)
MICTURITION DISORDER ( 3 FDA reports)
MIDDLE INSOMNIA ( 3 FDA reports)
MIOSIS ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MOUTH ULCERATION ( 3 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 3 FDA reports)
MUSCLE CONTRACTURE ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
MUSCLE TWITCHING ( 3 FDA reports)
MYELITIS TRANSVERSE ( 3 FDA reports)
MYOCLONUS ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
NO ADVERSE EVENT ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
NODULE ON EXTREMITY ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
NON-CONSUMMATION ( 3 FDA reports)
OESOPHAGEAL SPASM ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
OPTIC NEURITIS ( 3 FDA reports)
ORAL MUCOSA EROSION ( 3 FDA reports)
OSTECTOMY ( 3 FDA reports)
OSTEOCHONDROSIS ( 3 FDA reports)
OVARIAN CYST ( 3 FDA reports)
PAIN OF SKIN ( 3 FDA reports)
PARANEOPLASTIC SYNDROME ( 3 FDA reports)
PATHOLOGICAL FRACTURE ( 3 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 3 FDA reports)
PEMPHIGOID ( 3 FDA reports)
PERIODONTITIS ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PIGMENTATION DISORDER ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
POLYMYALGIA RHEUMATICA ( 3 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 3 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 3 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 3 FDA reports)
PROSTATE CANCER METASTATIC ( 3 FDA reports)
PSYCHOLOGICAL TRAUMA ( 3 FDA reports)
PSYCHOMOTOR RETARDATION ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
PURULENT DISCHARGE ( 3 FDA reports)
RADIOTHERAPY ( 3 FDA reports)
RADIUS FRACTURE ( 3 FDA reports)
RED BLOOD CELL COUNT ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
RESTLESS LEGS SYNDROME ( 3 FDA reports)
RETROPERITONEAL NEOPLASM ( 3 FDA reports)
RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
SCAR EXCISION ( 3 FDA reports)
SENSATION OF FOREIGN BODY ( 3 FDA reports)
SEQUESTRECTOMY ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SHOULDER OPERATION ( 3 FDA reports)
SKIN DISCOMFORT ( 3 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 3 FDA reports)
SOFT TISSUE INJURY ( 3 FDA reports)
SPINAL CORD NEOPLASM ( 3 FDA reports)
SPINAL OSTEOARTHRITIS ( 3 FDA reports)
SPINAL ROD INSERTION ( 3 FDA reports)
SPLENECTOMY ( 3 FDA reports)
STARING ( 3 FDA reports)
STOMATITIS NECROTISING ( 3 FDA reports)
SUDDEN CARDIAC DEATH ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
TERMINAL STATE ( 3 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 3 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 3 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 3 FDA reports)
TOOTH ABSCESS ( 3 FDA reports)
TOOTHACHE ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
UTERINE INFECTION ( 3 FDA reports)
VARICOSE VEIN ( 3 FDA reports)
VASCULITIS CEREBRAL ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
VERTEBROPLASTY ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
VITAMIN B12 ABNORMAL ( 3 FDA reports)
VITAMIN D DECREASED ( 3 FDA reports)
WAXY FLEXIBILITY ( 3 FDA reports)
WEIGHT BEARING DIFFICULTY ( 3 FDA reports)
WHITE BLOOD CELL COUNT ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABDOMINAL MASS ( 2 FDA reports)
ABDOMINAL OPERATION ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACCIDENT AT WORK ( 2 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 2 FDA reports)
ACTINIC KERATOSIS ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
ARTERY DISSECTION ( 2 FDA reports)
ARTHRITIS REACTIVE ( 2 FDA reports)
ARTIFICIAL ANUS ( 2 FDA reports)
ASEPTIC NECROSIS BONE ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BILIARY CIRRHOSIS ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
BLADDER PAIN ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BODY MASS INDEX INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE LESION ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BURSA DISORDER ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 2 FDA reports)
CATARACT OPERATION ( 2 FDA reports)
CHLAMYDIA SEROLOGY POSITIVE ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHONDROCALCINOSIS ( 2 FDA reports)
CLAVICLE FRACTURE ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CLUSTER HEADACHE ( 2 FDA reports)
COAGULATION TIME PROLONGED ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
COMPLEX PARTIAL SEIZURES ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
COOMBS TEST POSITIVE ( 2 FDA reports)
CRANIOTOMY ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
CULTURE WOUND POSITIVE ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYSTOCELE ( 2 FDA reports)
CYTOREDUCTIVE SURGERY ( 2 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DESMOID TUMOUR ( 2 FDA reports)
DIABETES MELLITUS MALNUTRITION-RELATED ( 2 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DISSOCIATION ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
EAR CONGESTION ( 2 FDA reports)
EATING DISORDER SYMPTOM ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
ENCEPHALOMALACIA ( 2 FDA reports)
ENDOMETRITIS ( 2 FDA reports)
ENTEROCUTANEOUS FISTULA ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EUSTACHIAN TUBE DISORDER ( 2 FDA reports)
EXPOSURE TO TOXIC AGENT ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
FAT NECROSIS ( 2 FDA reports)
FEAR OF NEEDLES ( 2 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 2 FDA reports)
FIBRINOLYSIS INCREASED ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FRACTURED SACRUM ( 2 FDA reports)
FROSTBITE ( 2 FDA reports)
FUNGAL OESOPHAGITIS ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GASTRIC PERFORATION ( 2 FDA reports)
GASTRIC POLYPS ( 2 FDA reports)
GASTRITIS FUNGAL ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 2 FDA reports)
GINGIVAL DISORDER ( 2 FDA reports)
GINGIVAL INFECTION ( 2 FDA reports)
GINGIVAL ULCERATION ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GOUTY ARTHRITIS ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HAND DEFORMITY ( 2 FDA reports)
HEMIANOPIA HOMONYMOUS ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HERPES PHARYNGITIS ( 2 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 2 FDA reports)
HERPES ZOSTER OTICUS ( 2 FDA reports)
HOSTILITY ( 2 FDA reports)
HUNGER ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTROPHIC OSTEOARTHROPATHY ( 2 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
HYPOREFLEXIA ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
ILLUSION ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INCISION SITE PAIN ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INJECTION SITE ABSCESS ( 2 FDA reports)
INJECTION SITE COLDNESS ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 2 FDA reports)
INTESTINAL STOMA ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
IRON OVERLOAD ( 2 FDA reports)
JAW FRACTURE ( 2 FDA reports)
JOINT CREPITATION ( 2 FDA reports)
JUGULAR VEIN THROMBOSIS ( 2 FDA reports)
KNEE OPERATION ( 2 FDA reports)
KYPHOSIS ( 2 FDA reports)
LARYNGEAL CANCER ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LIGAMENT LAXITY ( 2 FDA reports)
LIGAMENT RUPTURE ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LIPID METABOLISM DISORDER ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LYMPHADENECTOMY ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
METAPLASIA ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MINERAL SUPPLEMENTATION ( 2 FDA reports)
MOTION SICKNESS ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MYCOSIS FUNGOIDES ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOCARDIAL FIBROSIS ( 2 FDA reports)
NAIL HYPERTROPHY ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NECK MASS ( 2 FDA reports)
NEOPLASM SKIN ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NODULE ( 2 FDA reports)
NORMAL NEWBORN ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OPEN FRACTURE ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
OPTIC DISCS BLURRED ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
ORGASM ABNORMAL ( 2 FDA reports)
ORTHOSTATIC INTOLERANCE ( 2 FDA reports)
OSTEOMALACIA ( 2 FDA reports)
OSTEOPOROTIC FRACTURE ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PARATHYROID TUMOUR BENIGN ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PENIS DISORDER ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
PNEUMOPERITONEUM ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
PORPHYRIA ( 2 FDA reports)
PORPHYRIA NON-ACUTE ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
POST THROMBOTIC SYNDROME ( 2 FDA reports)
POST VIRAL FATIGUE SYNDROME ( 2 FDA reports)
POSTOPERATIVE ILEUS ( 2 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PROCTOCOLITIS ( 2 FDA reports)
PRODUCT CONTAINER ISSUE ( 2 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PSEUDOMENINGOCELE ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
PULMONARY TOXICITY ( 2 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 2 FDA reports)
PUSTULAR PSORIASIS ( 2 FDA reports)
QUALITY OF LIFE DECREASED ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RECTOCELE ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RETINAL VASCULAR DISORDER ( 2 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 2 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 2 FDA reports)
SKIN ATROPHY ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 2 FDA reports)
SPINAL PAIN ( 2 FDA reports)
STEROID THERAPY ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SUBCUTANEOUS NODULE ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
TOBACCO USER ( 2 FDA reports)
TOE AMPUTATION ( 2 FDA reports)
TONSIL CANCER ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TUMOUR PAIN ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
ULNAR TUNNEL SYNDROME ( 2 FDA reports)
URINARY TRACT DISORDER ( 2 FDA reports)
URINE ABNORMALITY ( 2 FDA reports)
URINE ODOUR ABNORMAL ( 2 FDA reports)
UROBILINOGEN URINE INCREASED ( 2 FDA reports)
VAGINAL FISTULA ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VARICES OESOPHAGEAL ( 2 FDA reports)
VASCULAR ACCESS COMPLICATION ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VENOOCCLUSIVE DISEASE ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
VITAMIN D DEFICIENCY ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
XEROSIS ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ABULIA ( 1 FDA reports)
ACARIASIS ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
AIRWAY PEAK PRESSURE INCREASED ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANALGESIC THERAPY ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANEURYSM REPAIR ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTIDIURETIC HORMONE ABNORMALITY ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE PAPULES ( 1 FDA reports)
APPLICATION SITE PARAESTHESIA ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
APPLICATION SITE WARMTH ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
AURA ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 1 FDA reports)
BASOPHIL COUNT INCREASED ( 1 FDA reports)
BED REST ( 1 FDA reports)
BENIGN LUNG NEOPLASM ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BIOPSY BONE ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLADDER PROLAPSE ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BONE DEBRIDEMENT ( 1 FDA reports)
BONE FISSURE ( 1 FDA reports)
BONE FORMATION DECREASED ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE MARROW OEDEMA SYNDROME ( 1 FDA reports)
BONE NEOPLASM MALIGNANT ( 1 FDA reports)
BONE TRIMMING ( 1 FDA reports)
BRADYCARDIA FOETAL ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX INFECTION ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARCINOMA IN SITU OF EYE ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERY BYPASS ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL HAEMANGIOMA ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL VASOCONSTRICTION ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CERUMEN IMPACTION ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHONDROMATOSIS ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COELIAC ARTERY STENOSIS ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COGNITIVE DETERIORATION ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLLATERAL CIRCULATION ( 1 FDA reports)
COMMINUTED FRACTURE ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CORRECTIVE LENS USER ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYSTITIS GLANDULARIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DENTAL DISCOMFORT ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DETOXIFICATION ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRESSLER'S SYNDROME ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
EAR INJURY ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
EDENTULOUS ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENCEPHALITIS PERIAXIALIS DIFFUSA ( 1 FDA reports)
ENDOCARDIAL FIBROSIS ( 1 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FAECALITH ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FRACTURE MALUNION ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
GALLBLADDER PAIN ( 1 FDA reports)
GASTRIC CANCER STAGE IV ( 1 FDA reports)
GASTRIC OPERATION ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL SURGERY ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN S INCREASED ( 1 FDA reports)
HAEMOPHILIA ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HIGH RISK PREGNANCY ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOPHARYNGEAL CANCER ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILLOGICAL THINKING ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INCISION SITE BLISTER ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCISION SITE OEDEMA ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFESTATION ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 1 FDA reports)
INTENSIVE CARE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
IRON BINDING CAPACITY UNSATURATED INCREASED ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAW OPERATION ( 1 FDA reports)
JOINT DESTRUCTION ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 1 FDA reports)
LAPAROSCOPY ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LITHOTRIPSY ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG NEOPLASM SURGERY ( 1 FDA reports)
LUPUS ENCEPHALITIS ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST NEGATIVE ( 1 FDA reports)
MALARIA ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MARFAN'S SYNDROME ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEDIASTINAL SHIFT ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MEDICAL DEVICE REMOVAL ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
METASTASES TO EYE ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
METASTATIC PAIN ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MOLE EXCISION ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE OPERATION ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYELOCYTE COUNT INCREASED ( 1 FDA reports)
MYELOMA RECURRENCE ( 1 FDA reports)
MYOSITIS OSSIFICANS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROSURGERY ( 1 FDA reports)
NEUTROPENIC INFECTION ( 1 FDA reports)
NIPPLE NEOPLASM ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
NUCLEATED RED CELLS ( 1 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL INJURY ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
ONYCHOMALACIA ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 1 FDA reports)
ORAL CAVITY FISTULA ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
OSTEOMA ( 1 FDA reports)
OXYGEN SUPPLEMENTATION ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL NERVE LESION ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERITONEAL TUBERCULOSIS ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PERITONITIS SCLEROSING ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHYSICAL DISABILITY ( 1 FDA reports)
PINGUECULA ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
PORPHYRIA ACUTE ( 1 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTPARTUM HYPOPITUITARISM ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROCEDURAL NAUSEA ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PROMYELOCYTE COUNT INCREASED ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PUBIC PAIN ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RADIATION MUCOSITIS ( 1 FDA reports)
RADICULAR CYST ( 1 FDA reports)
RADICULAR PAIN ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
REMOVAL OF INTERNAL FIXATION ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SACROILIITIS ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCROTAL ULCER ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUSITIS ASPERGILLUS ( 1 FDA reports)
SKIN CANCER METASTATIC ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN HYPOPIGMENTATION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPINAL ANAESTHESIA ( 1 FDA reports)
SPINAL COLUMN INJURY ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYMPTOM MASKED ( 1 FDA reports)
SYNOVECTOMY ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THERAPY RESPONDER ( 1 FDA reports)
THORACIC CAVITY DRAINAGE ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TOE DEFORMITY ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOOTH HYPOPLASIA ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TRAUMATIC FRACTURE ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TUMOUR COMPRESSION ( 1 FDA reports)
TUMOUR FLARE ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
UNEQUAL LIMB LENGTH ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URAEMIC ENCEPHALOPATHY ( 1 FDA reports)
URETERAL DIVERTICULUM ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VENOUS VALVE RUPTURED ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
VICTIM OF HOMICIDE ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
VULVOVAGINAL INJURY ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WEIGHT ABNORMAL ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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