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

FATIGUE ( 37 FDA reports)
HYPERTENSION ( 33 FDA reports)
CEREBROVASCULAR ACCIDENT ( 31 FDA reports)
DIARRHOEA ( 31 FDA reports)
HEADACHE ( 31 FDA reports)
BLOOD PRESSURE INCREASED ( 30 FDA reports)
MALAISE ( 30 FDA reports)
DIZZINESS ( 29 FDA reports)
NAUSEA ( 29 FDA reports)
CHEST PAIN ( 26 FDA reports)
FALL ( 26 FDA reports)
VOMITING ( 26 FDA reports)
DYSPNOEA ( 25 FDA reports)
PAIN ( 25 FDA reports)
WEIGHT DECREASED ( 25 FDA reports)
DECREASED APPETITE ( 24 FDA reports)
PYREXIA ( 23 FDA reports)
ABDOMINAL PAIN ( 22 FDA reports)
DEATH ( 20 FDA reports)
ATRIAL FIBRILLATION ( 19 FDA reports)
HEART RATE INCREASED ( 18 FDA reports)
HYPOAESTHESIA ( 18 FDA reports)
BLOOD CREATININE INCREASED ( 17 FDA reports)
LOSS OF CONSCIOUSNESS ( 17 FDA reports)
ABDOMINAL PAIN UPPER ( 16 FDA reports)
ANAEMIA ( 16 FDA reports)
ASTHENIA ( 15 FDA reports)
PRURITUS ( 15 FDA reports)
BACK PAIN ( 14 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 14 FDA reports)
ERYTHEMA ( 14 FDA reports)
FEELING ABNORMAL ( 14 FDA reports)
HYPOTENSION ( 14 FDA reports)
MYALGIA ( 14 FDA reports)
OFF LABEL USE ( 14 FDA reports)
RASH ( 14 FDA reports)
VISION BLURRED ( 14 FDA reports)
ABDOMINAL DISCOMFORT ( 13 FDA reports)
GAIT DISTURBANCE ( 13 FDA reports)
RENAL CYST ( 13 FDA reports)
SPINAL OSTEOARTHRITIS ( 13 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 12 FDA reports)
CELLULITIS ( 12 FDA reports)
DRUG INEFFECTIVE ( 12 FDA reports)
LOOSE TOOTH ( 12 FDA reports)
OEDEMA PERIPHERAL ( 12 FDA reports)
APHASIA ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
CONSTIPATION ( 11 FDA reports)
DEPRESSION ( 11 FDA reports)
HIATUS HERNIA ( 11 FDA reports)
OSTEONECROSIS OF JAW ( 11 FDA reports)
OSTEOPENIA ( 11 FDA reports)
THROMBOCYTOPENIA ( 11 FDA reports)
BLOOD POTASSIUM DECREASED ( 10 FDA reports)
DYSARTHRIA ( 10 FDA reports)
HAEMORRHAGE ( 10 FDA reports)
HYPERLIPIDAEMIA ( 10 FDA reports)
HYPERTENSIVE CRISIS ( 10 FDA reports)
NEPHROLITHIASIS ( 10 FDA reports)
SYNCOPE ( 10 FDA reports)
URINARY TRACT INFECTION ( 10 FDA reports)
BONE DISORDER ( 9 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 9 FDA reports)
CONTUSION ( 9 FDA reports)
COUGH ( 9 FDA reports)
DIVERTICULUM ( 9 FDA reports)
GINGIVAL BLEEDING ( 9 FDA reports)
GINGIVITIS ( 9 FDA reports)
HYPOPHAGIA ( 9 FDA reports)
ORAL INFECTION ( 9 FDA reports)
ORAL PAIN ( 9 FDA reports)
PAIN IN JAW ( 9 FDA reports)
PULMONARY HYPERTENSION ( 9 FDA reports)
RENAL FAILURE ACUTE ( 9 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 9 FDA reports)
TRISMUS ( 9 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 8 FDA reports)
ARRHYTHMIA ( 8 FDA reports)
ARTHRALGIA ( 8 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 8 FDA reports)
CHEST DISCOMFORT ( 8 FDA reports)
CONVULSION ( 8 FDA reports)
DRUG TOXICITY ( 8 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 8 FDA reports)
LYMPHADENOPATHY ( 8 FDA reports)
MITRAL VALVE INCOMPETENCE ( 8 FDA reports)
MUSCULAR WEAKNESS ( 8 FDA reports)
NEUROPATHY PERIPHERAL ( 8 FDA reports)
PAIN IN EXTREMITY ( 8 FDA reports)
PANCYTOPENIA ( 8 FDA reports)
PULMONARY CONGESTION ( 8 FDA reports)
TOOTH EXTRACTION ( 8 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 8 FDA reports)
AMNESIA ( 7 FDA reports)
ANXIETY ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 7 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 7 FDA reports)
DIASTOLIC DYSFUNCTION ( 7 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
DYSPNOEA EXERTIONAL ( 7 FDA reports)
FEELING HOT ( 7 FDA reports)
GINGIVAL INFECTION ( 7 FDA reports)
HAEMATURIA ( 7 FDA reports)
HYPERHIDROSIS ( 7 FDA reports)
HYPOGLYCAEMIA ( 7 FDA reports)
INFLUENZA LIKE ILLNESS ( 7 FDA reports)
INJURY ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 7 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 7 FDA reports)
OSTEOMYELITIS ( 7 FDA reports)
OSTEONECROSIS ( 7 FDA reports)
PERIODONTAL DISEASE ( 7 FDA reports)
PLEURAL EFFUSION ( 7 FDA reports)
PRIMARY SEQUESTRUM ( 7 FDA reports)
RASH PAPULAR ( 7 FDA reports)
SINUSITIS ( 7 FDA reports)
SKIN DISCOLOURATION ( 7 FDA reports)
SKIN EXFOLIATION ( 7 FDA reports)
SOMNOLENCE ( 7 FDA reports)
SQUAMOUS CELL CARCINOMA ( 7 FDA reports)
TOOTH FRACTURE ( 7 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 7 FDA reports)
WOUND ( 7 FDA reports)
ANGINA PECTORIS ( 6 FDA reports)
ANHEDONIA ( 6 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 6 FDA reports)
BONE PAIN ( 6 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 6 FDA reports)
BREAST TENDERNESS ( 6 FDA reports)
CEREBRAL ATROPHY ( 6 FDA reports)
CEREBRAL INFARCTION ( 6 FDA reports)
CHOLELITHIASIS ( 6 FDA reports)
COMA ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
DERMAL CYST ( 6 FDA reports)
DISABILITY ( 6 FDA reports)
DYSSTASIA ( 6 FDA reports)
ENCEPHALOMALACIA ( 6 FDA reports)
GINGIVAL PAIN ( 6 FDA reports)
GINGIVAL RECESSION ( 6 FDA reports)
GLIOSIS ( 6 FDA reports)
HEAT EXHAUSTION ( 6 FDA reports)
HEPATIC CYST ( 6 FDA reports)
HOT FLUSH ( 6 FDA reports)
HYPOGEUSIA ( 6 FDA reports)
INFLUENZA ( 6 FDA reports)
INJECTION SITE PAIN ( 6 FDA reports)
LEUKOPENIA ( 6 FDA reports)
MENTAL IMPAIRMENT ( 6 FDA reports)
MUCOSAL INFLAMMATION ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
MUSCLE STRAIN ( 6 FDA reports)
NASAL ODOUR ( 6 FDA reports)
NEUTROPENIA ( 6 FDA reports)
PAROTID GLAND ENLARGEMENT ( 6 FDA reports)
PULMONARY OEDEMA ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
RENAL IMPAIRMENT ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
SALIVARY GLAND PAIN ( 6 FDA reports)
SINUS DISORDER ( 6 FDA reports)
SPINAL HAEMANGIOMA ( 6 FDA reports)
SPONDYLOPATHY TRAUMATIC ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
TENDONITIS ( 6 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 6 FDA reports)
TOOTHACHE ( 6 FDA reports)
UNDERDOSE ( 6 FDA reports)
URINARY HESITATION ( 6 FDA reports)
AGEUSIA ( 5 FDA reports)
ASCITES ( 5 FDA reports)
BLADDER DISORDER ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
BLOOD POTASSIUM INCREASED ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
BODY TEMPERATURE INCREASED ( 5 FDA reports)
BREAST CANCER IN SITU ( 5 FDA reports)
BREAST CYST ( 5 FDA reports)
BREAST HYPERPLASIA ( 5 FDA reports)
BREAST MASS ( 5 FDA reports)
BREAST RECONSTRUCTION ( 5 FDA reports)
CREPITATIONS ( 5 FDA reports)
DERMATITIS EXFOLIATIVE ( 5 FDA reports)
ENTEROCOLITIS ( 5 FDA reports)
EOSINOPHILIA ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
HYPERTONIC BLADDER ( 5 FDA reports)
IMPAIRED HEALING ( 5 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 5 FDA reports)
INJECTION SITE DISCOLOURATION ( 5 FDA reports)
INJECTION SITE MASS ( 5 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
JUGULAR VEIN DISTENSION ( 5 FDA reports)
LUMBAR SPINAL STENOSIS ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
MASTECTOMY ( 5 FDA reports)
MENISCUS LESION ( 5 FDA reports)
METASTASES TO BONE ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
NEOPLASM MALIGNANT ( 5 FDA reports)
NEUROGENIC BLADDER ( 5 FDA reports)
NIGHT SWEATS ( 5 FDA reports)
OESOPHAGEAL PAIN ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
RENAL MASS ( 5 FDA reports)
RENAL TUMOUR EXCISION ( 5 FDA reports)
SKIN CANCER ( 5 FDA reports)
SURGERY ( 5 FDA reports)
TREMOR ( 5 FDA reports)
URINARY INCONTINENCE ( 5 FDA reports)
WOUND CLOSURE ( 5 FDA reports)
5-HYDROXYINDOLACETIC ACID INCREASED ( 4 FDA reports)
ABASIA ( 4 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
ANKLE FRACTURE ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 4 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 4 FDA reports)
BLOOD SODIUM DECREASED ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DRUG LEVEL INCREASED ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
EYE INFLAMMATION ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
GLAUCOMA ( 4 FDA reports)
HYPOKINESIA ( 4 FDA reports)
IMPETIGO ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
LEUKOCYTOSIS ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
METASTASES TO LIVER ( 4 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 4 FDA reports)
MYOPATHY ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
NEOPLASM PROGRESSION ( 4 FDA reports)
NERVOUSNESS ( 4 FDA reports)
NEUROTOXICITY ( 4 FDA reports)
PANCREATIC CYST ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
SKIN NEOPLASM EXCISION ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
WHEELCHAIR USER ( 4 FDA reports)
ATELECTASIS ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
BLEPHARITIS ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BONE DENSITY DECREASED ( 3 FDA reports)
BONE LOSS ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 3 FDA reports)
BREAST CALCIFICATIONS ( 3 FDA reports)
BREAST COSMETIC SURGERY ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
COMPRESSION FRACTURE ( 3 FDA reports)
DEBRIDEMENT ( 3 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
ERYTHEMA MULTIFORME ( 3 FDA reports)
EYE OEDEMA ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 3 FDA reports)
GROIN PAIN ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HEPATECTOMY ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HIP FRACTURE ( 3 FDA reports)
HYPERLIPASAEMIA ( 3 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
KNEE MENISCECTOMY ( 3 FDA reports)
LEUKAEMIA ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 3 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
MOUTH ULCERATION ( 3 FDA reports)
MUCOUS MEMBRANE DISORDER ( 3 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 3 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 3 FDA reports)
NUCLEATED RED CELLS ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
ORAL INTAKE REDUCED ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PANCREATIC DISORDER ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PARACENTESIS ( 3 FDA reports)
PELVIC PAIN ( 3 FDA reports)
PERONEAL NERVE PALSY ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
RENAL CELL CARCINOMA ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RENAL PAIN ( 3 FDA reports)
SCROTAL INFECTION ( 3 FDA reports)
SCROTAL PAIN ( 3 FDA reports)
SKIN LESION ( 3 FDA reports)
TOOTH REPAIR ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABDOMINAL SYMPTOM ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ACANTHOSIS ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ALPHA 1 MICROGLOBULIN INCREASED ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
AMBLYOPIA ( 2 FDA reports)
ANOXIC ENCEPHALOPATHY ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BIOPSY BREAST ( 2 FDA reports)
BIOPSY SKIN ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BONE LESION ( 2 FDA reports)
BRAIN STEM HAEMORRHAGE ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CATARACT OPERATION ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CERUMEN IMPACTION ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
COAGULATION TIME PROLONGED ( 2 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CREATININE URINE INCREASED ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DENTAL PROSTHESIS USER ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FLIGHT OF IDEAS ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
GASTROINTESTINAL SURGERY ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HIP SURGERY ( 2 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
ILEUS ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 2 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LAPAROTOMY ( 2 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LIVER TRANSPLANT REJECTION ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MAMMOPLASTY ( 2 FDA reports)
MENISCUS REMOVAL ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NEPHRITIS ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
OSTEOSCLEROSIS ( 2 FDA reports)
OTITIS MEDIA ACUTE ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PERIODONTITIS ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY GRANULOMA ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
RADIOTHERAPY ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SCAB ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SEQUESTRECTOMY ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN MASS ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
ULCER ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
URINE ODOUR ABNORMAL ( 2 FDA reports)
VASCULAR DEMENTIA ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
AORTIC RUPTURE ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
ARTERIAL INJURY ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BENIGN BONE NEOPLASM ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BIOPSY COLON ABNORMAL ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BONE CYST ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BREAST INDURATION ( 1 FDA reports)
BREAST LUMP REMOVAL ( 1 FDA reports)
BREAST MICROCALCIFICATION ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CAMPYLOBACTER INFECTION ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CARDIAC MYXOMA ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CATHETERISATION VENOUS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
DEMENTIA WITH LEWY BODIES ( 1 FDA reports)
DENTAL DISCOMFORT ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
EPISCLERITIS ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GLARE ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMANGIOMA CONGENITAL ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
IMMOBILISATION PROLONGED ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJURY CORNEAL ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
ITCHING SCAR ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALIGNANT TUMOUR EXCISION ( 1 FDA reports)
MASS EXCISION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO KIDNEY ( 1 FDA reports)
METASTASES TO STOMACH ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOTONIA ( 1 FDA reports)
NECROTISING ULCERATIVE PERIODONTITIS ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NODULE ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHLEBECTOMY ( 1 FDA reports)
PHYSICAL DISABILITY ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PNEUMONIA ESCHERICHIA ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHODOCOCCUS INFECTION ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCLERODERMA RENAL CRISIS ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SWEATING FEVER ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
TINEA CRURIS ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
ZYGOMYCOSIS ( 1 FDA reports)

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