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

FATIGUE ( 17 FDA reports)
NAUSEA ( 14 FDA reports)
ASTHENIA ( 13 FDA reports)
DIZZINESS ( 12 FDA reports)
FALL ( 11 FDA reports)
PYREXIA ( 11 FDA reports)
CHEST PAIN ( 10 FDA reports)
MYOCARDIAL INFARCTION ( 10 FDA reports)
VOMITING ( 10 FDA reports)
ANAEMIA ( 9 FDA reports)
CHILLS ( 9 FDA reports)
DIARRHOEA ( 9 FDA reports)
HAEMODIALYSIS ( 9 FDA reports)
HAEMOGLOBIN DECREASED ( 9 FDA reports)
HYPOTENSION ( 8 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 8 FDA reports)
VISION BLURRED ( 8 FDA reports)
ARTHRALGIA ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
CONTUSION ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
RENAL FAILURE ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
HAEMATOCHEZIA ( 6 FDA reports)
MALAISE ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
RASH ( 6 FDA reports)
ANOREXIA ( 5 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CARPAL TUNNEL SYNDROME ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
CORONARY ARTERY BYPASS ( 4 FDA reports)
CORONARY ARTERY OCCLUSION ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 4 FDA reports)
INJECTION SITE HAEMORRHAGE ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
PAIN ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
RENAL FAILURE CHRONIC ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
EYE SWELLING ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
MULTIPLE MYELOMA ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
NEPHRITIS INTERSTITIAL ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
OPERATIVE HAEMORRHAGE ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
TREMOR ( 3 FDA reports)
TROPONIN I INCREASED ( 3 FDA reports)
URATE NEPHROPATHY ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
AMNESIA ( 2 FDA reports)
ANAL DISCOMFORT ( 2 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
ARTERIAL STENOSIS ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
BLEPHARITIS ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
EAR HAEMORRHAGE ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEART VALVE REPLACEMENT ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
INFUSION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JOINT INSTABILITY ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LUMBAR SPINAL STENOSIS ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PROCEDURAL HYPOTENSION ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RETINAL ANEURYSM ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SWELLING ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VERTIGO POSITIONAL ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ADHESION ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL WALL THICKENING ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CANALITH REPOSITIONING PROCEDURE ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHONDROCALCINOSIS ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYST ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRINSIC ILIAC VEIN COMPRESSION ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GASTROINTESTINAL ULCER PERFORATION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GOUT ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE STINGING ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KERATOMILEUSIS ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MECHANICAL URTICARIA ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEDICATION TAMPERING ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
MILIA ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MONONEUROPATHY ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MORTON'S NEUROMA ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ONYCHALGIA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
PERINEPHRIC COLLECTION ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCIATIC NERVE INJURY ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY DECREASED ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPLENIC ARTERY ANEURYSM ( 1 FDA reports)
SPONDYLOARTHROPATHY ( 1 FDA reports)
STRESS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBTOTAL HYSTERECTOMY ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOE DEFORMITY ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VARICOSE VEIN RUPTURED ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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