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

COMPLETED SUICIDE ( 48 FDA reports)
DIARRHOEA ( 28 FDA reports)
VOMITING ( 27 FDA reports)
WEIGHT DECREASED ( 22 FDA reports)
SYNCOPE ( 21 FDA reports)
RESPIRATORY ARREST ( 19 FDA reports)
LOSS OF CONSCIOUSNESS ( 18 FDA reports)
GASTRITIS ( 17 FDA reports)
PNEUMONIA ( 17 FDA reports)
DUODENAL ULCER ( 16 FDA reports)
REFLUX OESOPHAGITIS ( 16 FDA reports)
DIZZINESS ( 15 FDA reports)
DYSPNOEA ( 15 FDA reports)
GASTROINTESTINAL DISORDER ( 15 FDA reports)
ANAEMIA ( 13 FDA reports)
DEATH ( 13 FDA reports)
MALAISE ( 13 FDA reports)
CARDIAC ARREST ( 12 FDA reports)
NAUSEA ( 12 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 11 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 11 FDA reports)
MYOCARDIAL INFARCTION ( 11 FDA reports)
CARDIO-RESPIRATORY ARREST ( 10 FDA reports)
SEPSIS ( 10 FDA reports)
ASTHENIA ( 9 FDA reports)
HAEMOGLOBIN DECREASED ( 9 FDA reports)
OEDEMA PERIPHERAL ( 9 FDA reports)
PYREXIA ( 9 FDA reports)
ALOPECIA ( 8 FDA reports)
CONTUSION ( 8 FDA reports)
ENTEROVESICAL FISTULA ( 8 FDA reports)
POISONING ( 8 FDA reports)
VISION BLURRED ( 8 FDA reports)
CEREBRAL HAEMORRHAGE ( 7 FDA reports)
DIVERTICULUM ( 7 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
FEMORAL NECK FRACTURE ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
HYPERSENSITIVITY ( 7 FDA reports)
HYPOTENSION ( 7 FDA reports)
RECTAL HAEMORRHAGE ( 7 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 7 FDA reports)
URINARY TRACT INFECTION ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 6 FDA reports)
BRONCHOPNEUMONIA ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
DRUG TOXICITY ( 6 FDA reports)
EYE DISORDER ( 6 FDA reports)
EYE PAIN ( 6 FDA reports)
INJURY ( 6 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE II ( 6 FDA reports)
MELAENA ( 6 FDA reports)
MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
PULSE ABSENT ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
BLOODY DISCHARGE ( 5 FDA reports)
CEREBROVASCULAR ACCIDENT ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
DRY EYE ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
FALL ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 5 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 5 FDA reports)
LENS DISORDER ( 5 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 5 FDA reports)
LUNG NEOPLASM MALIGNANT ( 5 FDA reports)
PALLOR ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
RHEUMATOID ARTHRITIS ( 5 FDA reports)
SINUSITIS ( 5 FDA reports)
SKIN BURNING SENSATION ( 5 FDA reports)
SKIN CANCER ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
ANAL CANCER ( 4 FDA reports)
BLINDNESS ( 4 FDA reports)
CARCINOMA IN SITU OF SKIN ( 4 FDA reports)
COLON CANCER ( 4 FDA reports)
COLON CANCER STAGE I ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
ILL-DEFINED DISORDER ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
INTENTIONAL MISUSE ( 4 FDA reports)
INTERVERTEBRAL DISCITIS ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER ( 4 FDA reports)
OESOPHAGITIS ULCERATIVE ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PULMONARY FIBROSIS ( 4 FDA reports)
PUPILLARY DISORDER ( 4 FDA reports)
PURPURA ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 4 FDA reports)
THYROID CANCER ( 4 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
BREAST CANCER ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CHOLECYSTECTOMY ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
COMA ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
EXTRADURAL ABSCESS ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
LARGE INTESTINAL ULCER ( 3 FDA reports)
LARYNGEAL CANCER ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
OESOPHAGEAL ADENOCARCINOMA METASTATIC ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
QUADRIPLEGIA ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
TREMOR ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ARTHRITIS BACTERIAL ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CAROTID ARTERY OCCLUSION ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CYST ( 2 FDA reports)
CYSTOCELE REPAIR ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTROINTESTINAL INJURY ( 2 FDA reports)
HAEMATOMA INFECTION ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HANGOVER ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HUNGER ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
MALIGNANT PALATE NEOPLASM ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
NASAL NEOPLASM ( 2 FDA reports)
NASAL SINUS CANCER ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
OCULAR NEOPLASM ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PAIN ( 2 FDA reports)
PERIDIVERTICULAR ABSCESS ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
RASH ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SYNOVIAL RUPTURE ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
ULCER ( 2 FDA reports)
VASCULAR DEMENTIA ( 2 FDA reports)
VENOUS HAEMORRHAGE ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WEIGHT GAIN POOR ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AURA ( 1 FDA reports)
AURICULAR PERICHONDRITIS ( 1 FDA reports)
AUTISM ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CORTISOL ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CSF GLUCOSE ABNORMAL ( 1 FDA reports)
CSF GLUCOSE DECREASED ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CYSTOSARCOMA PHYLLODES ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FELTY'S SYNDROME ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GASTRIC VOLVULUS ( 1 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE UNSPECIFIED ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG THERAPY ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT INJECTION ( 1 FDA reports)
JOINT PROSTHESIS USER ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MALIGNANT SOFT TISSUE NEOPLASM ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGORRHAGIA ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL ATRESIA ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OVARIAN ABSCESS ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHOBIA ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PSEUDODEMENTIA ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RETINAL ARTERY EMBOLISM ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RHEUMATOID VASCULITIS ( 1 FDA reports)
SALIVARY GLAND CANCER ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SICCA SYNDROME ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN SENSITISATION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
TAKAYASU'S ARTERITIS ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TONSIL CANCER ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TRACHEAL FISTULA ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRISOMY 21 ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITAMIN K DEFICIENCY ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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