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

DYSPNOEA ( 41 FDA reports)
RENAL FAILURE ACUTE ( 41 FDA reports)
ATRIAL FIBRILLATION ( 38 FDA reports)
OEDEMA PERIPHERAL ( 38 FDA reports)
PAIN ( 35 FDA reports)
CONFUSIONAL STATE ( 34 FDA reports)
HAEMOGLOBIN DECREASED ( 34 FDA reports)
VOMITING ( 34 FDA reports)
ERYTHEMA ( 33 FDA reports)
MALAISE ( 33 FDA reports)
NAUSEA ( 32 FDA reports)
DIARRHOEA ( 31 FDA reports)
HEADACHE ( 30 FDA reports)
FALL ( 27 FDA reports)
PRURITUS ( 27 FDA reports)
PNEUMONIA ( 26 FDA reports)
PYREXIA ( 26 FDA reports)
CHEST PAIN ( 25 FDA reports)
DEATH ( 25 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 25 FDA reports)
ARTHRALGIA ( 24 FDA reports)
DIZZINESS ( 23 FDA reports)
SEPSIS ( 23 FDA reports)
URINARY TRACT INFECTION ( 23 FDA reports)
BLOOD CREATININE INCREASED ( 22 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 22 FDA reports)
FLUID OVERLOAD ( 19 FDA reports)
STEVENS-JOHNSON SYNDROME ( 19 FDA reports)
HYPERSENSITIVITY ( 18 FDA reports)
RASH GENERALISED ( 18 FDA reports)
BLISTER ( 17 FDA reports)
HYPOKALAEMIA ( 17 FDA reports)
DRY SKIN ( 16 FDA reports)
ECZEMA ( 16 FDA reports)
EXFOLIATIVE RASH ( 16 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 16 FDA reports)
NEUTROPENIC SEPSIS ( 16 FDA reports)
RASH ( 16 FDA reports)
RASH MACULO-PAPULAR ( 16 FDA reports)
RASH PRURITIC ( 16 FDA reports)
SWELLING ( 16 FDA reports)
CARDIAC ARREST ( 15 FDA reports)
PETECHIAE ( 15 FDA reports)
SCAB ( 15 FDA reports)
DEEP VEIN THROMBOSIS ( 14 FDA reports)
DRUG INTERACTION ( 14 FDA reports)
AGITATION ( 13 FDA reports)
HAEMATEMESIS ( 13 FDA reports)
HEART RATE INCREASED ( 13 FDA reports)
HYPERTENSION ( 13 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 13 FDA reports)
NAIL DISORDER ( 13 FDA reports)
OESOPHAGEAL ULCER ( 13 FDA reports)
PULMONARY EMBOLISM ( 13 FDA reports)
RECTAL HAEMORRHAGE ( 13 FDA reports)
SWOLLEN TONGUE ( 13 FDA reports)
ASTHENIA ( 12 FDA reports)
CEREBROVASCULAR ACCIDENT ( 12 FDA reports)
CONDITION AGGRAVATED ( 12 FDA reports)
DEHYDRATION ( 12 FDA reports)
DRUG INEFFECTIVE ( 12 FDA reports)
HYPONATRAEMIA ( 12 FDA reports)
MELAENA ( 12 FDA reports)
NEUTROPENIA ( 12 FDA reports)
NEUTROPHIL COUNT DECREASED ( 12 FDA reports)
ONYCHOMYCOSIS ( 12 FDA reports)
SYNCOPE ( 12 FDA reports)
CHEST DISCOMFORT ( 11 FDA reports)
COUGH ( 11 FDA reports)
FATIGUE ( 11 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 11 FDA reports)
INSOMNIA ( 11 FDA reports)
PALLOR ( 11 FDA reports)
ABDOMINAL PAIN ( 10 FDA reports)
AMNESIA ( 10 FDA reports)
DYSARTHRIA ( 10 FDA reports)
INHIBITORY DRUG INTERACTION ( 10 FDA reports)
PAIN IN EXTREMITY ( 10 FDA reports)
SOMNOLENCE ( 10 FDA reports)
AGGRESSION ( 9 FDA reports)
ANXIETY ( 9 FDA reports)
CIRCULATORY COLLAPSE ( 9 FDA reports)
COLITIS ( 9 FDA reports)
CONVULSION ( 9 FDA reports)
CROHN'S DISEASE ( 9 FDA reports)
DEPRESSION ( 9 FDA reports)
HALLUCINATION ( 9 FDA reports)
HYPERKALAEMIA ( 9 FDA reports)
HYPOMAGNESAEMIA ( 9 FDA reports)
INFECTION ( 9 FDA reports)
INFLUENZA LIKE ILLNESS ( 9 FDA reports)
LOSS OF CONSCIOUSNESS ( 9 FDA reports)
MOBILITY DECREASED ( 9 FDA reports)
MUSCULOSKELETAL PAIN ( 9 FDA reports)
MYOCARDIAL INFARCTION ( 9 FDA reports)
PARAESTHESIA ( 9 FDA reports)
PULMONARY FIBROSIS ( 9 FDA reports)
RESPIRATORY FAILURE ( 9 FDA reports)
UNRESPONSIVE TO STIMULI ( 9 FDA reports)
WHEEZING ( 9 FDA reports)
ANAEMIA ( 8 FDA reports)
DYSPEPSIA ( 8 FDA reports)
HYPOCALCAEMIA ( 8 FDA reports)
HYPOTENSION ( 8 FDA reports)
MUSCULAR WEAKNESS ( 8 FDA reports)
MYALGIA ( 8 FDA reports)
OROPHARYNGEAL PAIN ( 8 FDA reports)
ORTHOSTATIC HYPOTENSION ( 8 FDA reports)
PALPITATIONS ( 8 FDA reports)
SKIN ULCER ( 8 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 8 FDA reports)
TREMOR ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 7 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 7 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 7 FDA reports)
HYPERHIDROSIS ( 7 FDA reports)
INCONTINENCE ( 7 FDA reports)
NECK PAIN ( 7 FDA reports)
RASH ERYTHEMATOUS ( 7 FDA reports)
SKIN EXFOLIATION ( 7 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 7 FDA reports)
VASCULITIS ( 7 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
CEREBRAL HAEMORRHAGE ( 6 FDA reports)
CLOSTRIDIAL INFECTION ( 6 FDA reports)
FLUSHING ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
HIATUS HERNIA ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
HYPOPHOSPHATAEMIA ( 6 FDA reports)
LETHARGY ( 6 FDA reports)
LUPUS-LIKE SYNDROME ( 6 FDA reports)
MEDICATION ERROR ( 6 FDA reports)
METABOLIC ACIDOSIS ( 6 FDA reports)
OSTEOPOROSIS ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
REFLUX OESOPHAGITIS ( 6 FDA reports)
RHEUMATOID ARTHRITIS ( 6 FDA reports)
VISUAL DISTURBANCE ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
ABSCESS ( 5 FDA reports)
ANGINA PECTORIS ( 5 FDA reports)
BALANCE DISORDER ( 5 FDA reports)
BLOOD CALCIUM DECREASED ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
CELLULITIS ( 5 FDA reports)
CHILLS ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
CORONARY ARTERY OCCLUSION ( 5 FDA reports)
DUODENAL ULCER ( 5 FDA reports)
DYSPHONIA ( 5 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 5 FDA reports)
ESCHERICHIA SEPSIS ( 5 FDA reports)
EYE PAIN ( 5 FDA reports)
EYE SWELLING ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
GRAND MAL CONVULSION ( 5 FDA reports)
HIP FRACTURE ( 5 FDA reports)
INFUSION RELATED REACTION ( 5 FDA reports)
INTENTIONAL DRUG MISUSE ( 5 FDA reports)
LYMPHOPENIA ( 5 FDA reports)
MENINGITIS LISTERIA ( 5 FDA reports)
METASTASES TO LUNG ( 5 FDA reports)
MIGRAINE ( 5 FDA reports)
MOUTH ULCERATION ( 5 FDA reports)
NEOPLASM MALIGNANT ( 5 FDA reports)
OSTEONECROSIS ( 5 FDA reports)
PERIPHERAL ISCHAEMIA ( 5 FDA reports)
PLEURAL DISORDER ( 5 FDA reports)
PSYCHOTIC DISORDER ( 5 FDA reports)
RASH PAPULAR ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
SKIN WARM ( 5 FDA reports)
THERAPY NON-RESPONDER ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
BACTERIAL SEPSIS ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
BLOOD SODIUM DECREASED ( 4 FDA reports)
BLOOD URINE ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CHOKING ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
COLITIS ULCERATIVE ( 4 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
ENCEPHALITIS ( 4 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 4 FDA reports)
FAECAL INCONTINENCE ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
HAIR GROWTH ABNORMAL ( 4 FDA reports)
HALLUCINATION, VISUAL ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
HICCUPS ( 4 FDA reports)
HYPERSEXUALITY ( 4 FDA reports)
HYPOTHERMIA ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
ISCHAEMIC STROKE ( 4 FDA reports)
JAUNDICE ( 4 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 4 FDA reports)
METABOLIC DISORDER ( 4 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
MUSCLE DISORDER ( 4 FDA reports)
NIGHT SWEATS ( 4 FDA reports)
OESOPHAGEAL CARCINOMA ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
PHARYNGEAL ERYTHEMA ( 4 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 4 FDA reports)
PSOAS ABSCESS ( 4 FDA reports)
SCIATICA ( 4 FDA reports)
SOFT TISSUE INFECTION ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
SUBDURAL HAEMATOMA ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 3 FDA reports)
BLEPHARITIS ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BLOOD SODIUM INCREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
BRAIN ABSCESS ( 3 FDA reports)
BREAST PAIN ( 3 FDA reports)
BRONCHOPNEUMONIA ( 3 FDA reports)
CAECITIS ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 3 FDA reports)
DYSLEXIA ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
ESCHERICHIA INFECTION ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FEMORAL NECK FRACTURE ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
INTERVERTEBRAL DISCITIS ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
LEUKOENCEPHALOPATHY ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
MACULAR DEGENERATION ( 3 FDA reports)
MECHANICAL VENTILATION ( 3 FDA reports)
MUCOSAL EROSION ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
ONYCHOLYSIS ( 3 FDA reports)
OROPHARYNGEAL SWELLING ( 3 FDA reports)
OSTEONECROSIS OF JAW ( 3 FDA reports)
PARANOIA ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PLEURITIC PAIN ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SKIN EROSION ( 3 FDA reports)
SKIN IRRITATION ( 3 FDA reports)
SKIN SWELLING ( 3 FDA reports)
SKIN TIGHTNESS ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VASCULITIC RASH ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
ABDOMINAL INJURY ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
AGORAPHOBIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
APATHY ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTHRITIS REACTIVE ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD ELECTROLYTES INCREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD OSMOLARITY DECREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREAST ENLARGEMENT ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DIABETIC FOOT ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DUODENAL ULCER PERFORATION ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSPNOEA AT REST ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FEMORAL ARTERY EMBOLISM ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROENTERITIS NOROVIRUS ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GLOBULINS INCREASED ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATOSPLENIC T-CELL LYMPHOMA ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
JOINT INJECTION ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LIVER TRANSPLANT ( 2 FDA reports)
MADAROSIS ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
MITRAL VALVE DISEASE ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NEOPLASM PROGRESSION ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POLYMYALGIA RHEUMATICA ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
POSTOPERATIVE ADHESION ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSORIATIC ARTHROPATHY ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RADIAL NERVE PALSY ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RETINAL VEIN OCCLUSION ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SYNOVITIS ( 2 FDA reports)
TENOSYNOVITIS ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URINE ELECTROLYTES ABNORMAL ( 2 FDA reports)
URINE OSMOLARITY INCREASED ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 2 FDA reports)
VASOCONSTRICTION ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD OESTROGEN DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CINCHONISM ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION POSTOPERATIVE ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GINGIVAL INFECTION ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPHYSITIS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL HYPERSEGMENTED MORPHOLOGY PRESENT ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
ORTHOPEDIC PROCEDURE ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARASPINAL ABSCESS ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PURPURA ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
REACTION TO PRESERVATIVES ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RESECTION OF RECTUM ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETICULOCYTOSIS ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SENSITISATION ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SURGERY ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOLYSIS ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TRIGEMINAL NERVE DISORDER ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
ULCER ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VAGINAL PROLAPSE ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
WOUND ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
YERSINIA INFECTION ( 1 FDA reports)

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