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

VOMITING ( 27 FDA reports)
DIARRHOEA ( 20 FDA reports)
PNEUMONIA ( 17 FDA reports)
DYSPNOEA ( 16 FDA reports)
FALL ( 16 FDA reports)
HAEMOGLOBIN DECREASED ( 16 FDA reports)
MALAISE ( 16 FDA reports)
DEATH ( 13 FDA reports)
HEADACHE ( 13 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 13 FDA reports)
ARTHRALGIA ( 12 FDA reports)
DIZZINESS ( 12 FDA reports)
JAUNDICE ( 12 FDA reports)
DECREASED APPETITE ( 11 FDA reports)
PYREXIA ( 11 FDA reports)
SEPSIS ( 11 FDA reports)
ERYTHEMA ( 10 FDA reports)
HYPOKALAEMIA ( 10 FDA reports)
URINARY TRACT INFECTION ( 10 FDA reports)
CONFUSIONAL STATE ( 9 FDA reports)
DRUG INEFFECTIVE ( 9 FDA reports)
OEDEMA PERIPHERAL ( 9 FDA reports)
RENAL FAILURE ACUTE ( 9 FDA reports)
NAUSEA ( 8 FDA reports)
RECTAL HAEMORRHAGE ( 8 FDA reports)
TREMOR ( 8 FDA reports)
ABDOMINAL PAIN ( 7 FDA reports)
BREAST CANCER METASTATIC ( 7 FDA reports)
CELLULITIS ( 7 FDA reports)
CROHN'S DISEASE ( 7 FDA reports)
DISEASE PROGRESSION ( 7 FDA reports)
DYSARTHRIA ( 7 FDA reports)
DYSURIA ( 7 FDA reports)
HERPES ZOSTER OTICUS ( 7 FDA reports)
INFECTION ( 7 FDA reports)
LETHARGY ( 7 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 7 FDA reports)
NEUTROPENIC SEPSIS ( 7 FDA reports)
PAIN ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
SOMNOLENCE ( 7 FDA reports)
VIITH NERVE PARALYSIS ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
COLITIS ISCHAEMIC ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
DEEP VEIN THROMBOSIS ( 6 FDA reports)
INHIBITORY DRUG INTERACTION ( 6 FDA reports)
RASH ERYTHEMATOUS ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 6 FDA reports)
VISION BLURRED ( 6 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
BRONCHOPNEUMONIA ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CEREBRAL INFARCTION ( 5 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 5 FDA reports)
ENCEPHALITIS ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HEPATIC NECROSIS ( 5 FDA reports)
HICCUPS ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
HYPOMAGNESAEMIA ( 5 FDA reports)
LUNG NEOPLASM MALIGNANT ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
RASH ( 5 FDA reports)
RHEUMATOID ARTHRITIS ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
AGGRESSION ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DIVERTICULITIS ( 4 FDA reports)
ECZEMA ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
FLUID OVERLOAD ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
ILL-DEFINED DISORDER ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
LUNG NEOPLASM ( 4 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
MOUTH ULCERATION ( 4 FDA reports)
NEOPLASM MALIGNANT ( 4 FDA reports)
NEUTROPHIL COUNT DECREASED ( 4 FDA reports)
OROPHARYNGEAL PAIN ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
PULMONARY FIBROSIS ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RASH PRURITIC ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
RENAL MASS ( 4 FDA reports)
SOFT TISSUE DISORDER ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BLOOD URINE ( 3 FDA reports)
BLOOD URINE PRESENT ( 3 FDA reports)
BRONCHIECTASIS ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
COELIAC DISEASE ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HODGKIN'S DISEASE MIXED CELLULARITY STAGE III ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NEURALGIA ( 3 FDA reports)
NIGHT SWEATS ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PHARYNGEAL ERYTHEMA ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
ARTHRITIS BACTERIAL ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BACTERIAL DISEASE CARRIER ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREAST PAIN ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARCINOID TUMOUR PULMONARY ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
EXFOLIATIVE RASH ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GALLBLADDER CANCER ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMOSTASIS ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HORDEOLUM ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MULTIPLE FRACTURES ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OSTEONECROSIS OF JAW ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMONIA MYCOPLASMAL ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
SCAB ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SWELLING ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
URINE ODOUR ABNORMAL ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ADMINISTRATION SITE PAIN ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ASBESTOSIS ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMA ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORNEAL GRAFT REJECTION ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 1 FDA reports)
DENTAL CARE ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEMORAL HERNIA ( 1 FDA reports)
FEMORAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACRIMAL DUCT PROCEDURE ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALARIA ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ONYCHOLYSIS ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEUROTHOTONUS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RALES ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL ONCOCYTOMA ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL ARTERY EMBOLISM ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYRINGE ISSUE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)
YOUNG'S SYNDROME ( 1 FDA reports)

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