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

DEATH ( 37 FDA reports)
DISEASE PROGRESSION ( 37 FDA reports)
PNEUMONIA ( 31 FDA reports)
PYREXIA ( 28 FDA reports)
DYSPNOEA ( 24 FDA reports)
INTERSTITIAL LUNG DISEASE ( 24 FDA reports)
RESPIRATORY FAILURE ( 20 FDA reports)
INFLUENZA LIKE ILLNESS ( 16 FDA reports)
NAUSEA ( 16 FDA reports)
ANAEMIA ( 15 FDA reports)
CHILLS ( 15 FDA reports)
FATIGUE ( 15 FDA reports)
CONDITION AGGRAVATED ( 14 FDA reports)
WEIGHT DECREASED ( 12 FDA reports)
ASTHENIA ( 11 FDA reports)
COUGH ( 10 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 10 FDA reports)
HYPOXIA ( 9 FDA reports)
PAIN ( 9 FDA reports)
TREMOR ( 9 FDA reports)
VOMITING ( 9 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 8 FDA reports)
RENAL FAILURE ( 8 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
DIARRHOEA ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 7 FDA reports)
INFECTION ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
NEUTROPENIA ( 7 FDA reports)
OXYGEN SATURATION DECREASED ( 7 FDA reports)
PULMONARY EMBOLISM ( 7 FDA reports)
PULMONARY FIBROSIS ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
ACUTE RESPIRATORY FAILURE ( 6 FDA reports)
ARTHRALGIA ( 6 FDA reports)
BACK PAIN ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
CELLULITIS ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
RESTLESSNESS ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
ANXIETY ( 5 FDA reports)
ASCITES ( 5 FDA reports)
CEREBROVASCULAR ACCIDENT ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
FALL ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
MALAISE ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 5 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
BLADDER CANCER ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
MENTAL STATUS CHANGES ( 4 FDA reports)
MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
TENDERNESS ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ANOREXIA ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
BLADDER OBSTRUCTION ( 3 FDA reports)
CATARACT ( 3 FDA reports)
COLONIC STENOSIS ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DEVICE FAILURE ( 3 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
FRACTURE ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
INJECTION SITE INFECTION ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LIVER ABSCESS ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
METASTASES TO LYMPH NODES ( 3 FDA reports)
NEUTROPENIC COLITIS ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PLEURAL FIBROSIS ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RALES ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
SPINAL COMPRESSION FRACTURE ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
THIRST ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BENIGN DUODENAL NEOPLASM ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CENTRAL LINE INFECTION ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COMA ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
COR PULMONALE ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPNOEA EXACERBATED ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
INTESTINAL FISTULA ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
LUNG TRANSPLANT ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MANTLE CELL LYMPHOMA ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
OESOPHAGEAL VARICEAL LIGATION ( 2 FDA reports)
OSTEOPETROSIS ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PITTING OEDEMA ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
WEIGHT FLUCTUATION ( 2 FDA reports)
X-RAY ABNORMAL ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADHESION ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ALVEOLITIS FIBROSING ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL NATRIURETIC PEPTIDE DECREASED ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BACTEROIDES INFECTION ( 1 FDA reports)
BENIGN SMALL INTESTINAL NEOPLASM ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE NEOPLASM MALIGNANT ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE DECREASED ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COMPLICATED FRACTURE ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
COXSACKIE MYOCARDITIS ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIAPHRAGM NEOPLASM ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOCARDITIS Q FEVER ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
EXERCISE CAPACITY DECREASED ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLUCTUANCE ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT RESECTABLE ( 1 FDA reports)
HIGH FREQUENCY ABLATION ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMOBILISATION PROLONGED ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE PHLEBITIS ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MYCOBACTERIUM ABSCESSUS INFECTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATECTOMY ( 1 FDA reports)
PANCREATIC CARCINOMA RECURRENT ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PERICARDIAL FIBROSIS ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLASMACYTOSIS ( 1 FDA reports)
PNEUMATOSIS ( 1 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSYCHOMOTOR AGITATION ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCEDOSPORIUM INFECTION ( 1 FDA reports)
SEBORRHOEA ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SINUSITIS ASPERGILLUS ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
THERAPEUTIC EMBOLISATION ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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