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

PYREXIA ( 31 FDA reports)
RENAL FAILURE ACUTE ( 22 FDA reports)
RENAL FAILURE ( 19 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 17 FDA reports)
VOMITING ( 17 FDA reports)
HEADACHE ( 16 FDA reports)
DYSPNOEA ( 15 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 15 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 15 FDA reports)
NEUROPATHY PERIPHERAL ( 15 FDA reports)
CYTOLYTIC HEPATITIS ( 14 FDA reports)
DIARRHOEA ( 14 FDA reports)
PRURITUS ( 14 FDA reports)
RASH ( 14 FDA reports)
APHASIA ( 13 FDA reports)
DIZZINESS ( 13 FDA reports)
HYPOAESTHESIA ( 13 FDA reports)
TACHYCARDIA ( 13 FDA reports)
DRUG INEFFECTIVE ( 12 FDA reports)
ANAEMIA ( 11 FDA reports)
CHEST PAIN ( 11 FDA reports)
ERYTHEMA NODOSUM ( 11 FDA reports)
PURPURA ( 11 FDA reports)
ASTHENIA ( 10 FDA reports)
MALAISE ( 10 FDA reports)
LOSS OF CONSCIOUSNESS ( 9 FDA reports)
MOUTH ULCERATION ( 9 FDA reports)
SOMNOLENCE ( 9 FDA reports)
THROMBOCYTOPENIA ( 9 FDA reports)
ARTHRALGIA ( 8 FDA reports)
DRUG INTERACTION ( 8 FDA reports)
ECCHYMOSIS ( 8 FDA reports)
GAIT DISTURBANCE ( 8 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 8 FDA reports)
RASH MACULO-PAPULAR ( 8 FDA reports)
TOXIC SKIN ERUPTION ( 8 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 7 FDA reports)
BLEEDING ANOVULATORY ( 7 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 7 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 7 FDA reports)
POLYNEUROPATHY ( 7 FDA reports)
RASH PAPULAR ( 7 FDA reports)
VISUAL ACUITY REDUCED ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ANGIOEDEMA ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
CROHN'S DISEASE ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
EOSINOPHIL COUNT INCREASED ( 6 FDA reports)
LUNG INFECTION ( 6 FDA reports)
MOTOR DYSFUNCTION ( 6 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
MULTIPLE SCLEROSIS ( 6 FDA reports)
NECROTISING OESOPHAGITIS ( 6 FDA reports)
NERVOUS SYSTEM DISORDER ( 6 FDA reports)
PROTEINURIA ( 6 FDA reports)
URTICARIA ( 6 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
COLITIS ( 5 FDA reports)
COUGH ( 5 FDA reports)
DYSPLASIA ( 5 FDA reports)
ECZEMA ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
GASTRIC HAEMORRHAGE ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
HYPONATRAEMIA ( 5 FDA reports)
IRON DEFICIENCY ANAEMIA ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
LIVER INJURY ( 5 FDA reports)
METABOLIC ACIDOSIS ( 5 FDA reports)
MUSCLE SPASTICITY ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
PSORIASIS ( 5 FDA reports)
SENSORY DISTURBANCE ( 5 FDA reports)
THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
TONSILLITIS ( 5 FDA reports)
UVEITIS ( 5 FDA reports)
VERTIGO ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
CANDIDA SEPSIS ( 4 FDA reports)
CHOROIDITIS ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 4 FDA reports)
CYSTITIS ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DEMYELINATION ( 4 FDA reports)
DRUG ABUSE ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
FALL ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
GRANULOMA ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
HYPOKINESIA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
INTERMEDIATE UVEITIS ( 4 FDA reports)
IRIDOCYCLITIS ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
LYMPHOPENIA ( 4 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PULMONARY FIBROSIS ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
SPASTIC PARAPLEGIA ( 4 FDA reports)
TOXIC ENCEPHALOPATHY ( 4 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 4 FDA reports)
VESSEL PUNCTURE SITE REACTION ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
AGITATION ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
INCOHERENT ( 3 FDA reports)
INTRA-UTERINE DEATH ( 3 FDA reports)
MENINGOCELE ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
OPTIC NEURITIS ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PUSTULAR PSORIASIS ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SKIN INFLAMMATION ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BIOPSY SKIN ABNORMAL ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CELL DEATH ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 2 FDA reports)
FOLATE DEFICIENCY ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GUTTATE PSORIASIS ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HOMOCYSTINAEMIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MICROALBUMINURIA ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PARAKERATOSIS ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PNEUMOCOCCAL SEPSIS ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PSORIATIC ARTHROPATHY ( 2 FDA reports)
RETINAL VEIN THROMBOSIS ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
SAPHO SYNDROME ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
TRAUMATIC HAEMATOMA ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
VASCULITIS CEREBRAL ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACROMEGALY ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
AQUAGENIC PRURITUS ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CROSS SENSITIVITY REACTION ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DERMATOPHYTOSIS ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EPIDERMOLYSIS BULLOSA ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FELTY'S SYNDROME ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FUNGAL CYSTITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
KAOLIN CEPHALIN CLOTTING TIME ABNORMAL ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 1 FDA reports)
PHLEBITIS DEEP ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RASH SCARLATINIFORM ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SKIN MACERATION ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
ULCER ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)

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