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INFUSION RELATED REACTION ( 27 FDA reports)
DYSPNOEA ( 16 FDA reports)
DRUG INEFFECTIVE ( 13 FDA reports)
MALAISE ( 13 FDA reports)
PAIN ( 12 FDA reports)
FATIGUE ( 11 FDA reports)
NAUSEA ( 10 FDA reports)
HEADACHE ( 9 FDA reports)
PNEUMONIA ( 9 FDA reports)
VOMITING ( 9 FDA reports)
ABDOMINAL PAIN ( 8 FDA reports)
BACK PAIN ( 8 FDA reports)
CROHN'S DISEASE ( 8 FDA reports)
FLUSHING ( 8 FDA reports)
ASTHENIA ( 7 FDA reports)
DIARRHOEA ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
HYPERSENSITIVITY ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
SUICIDE ATTEMPT ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 7 FDA reports)
ABDOMINAL HERNIA ( 6 FDA reports)
ADVERSE DRUG REACTION ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
CHILLS ( 6 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
PULMONARY EMBOLISM ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 6 FDA reports)
WOUND INFECTION ( 6 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
COUGH ( 5 FDA reports)
DISSEMINATED TUBERCULOSIS ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
DRUG EFFECT DECREASED ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
OXYGEN SATURATION DECREASED ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
PRODUCT ADHESION ISSUE ( 5 FDA reports)
RASH ( 5 FDA reports)
ROAD TRAFFIC ACCIDENT ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
ACNE ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
COLITIS ULCERATIVE ( 4 FDA reports)
DERMATITIS CONTACT ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
INFECTION ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
MULTIPLE SCLEROSIS ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
SJOGREN'S SYNDROME ( 4 FDA reports)
SLUGGISHNESS ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
SURGERY ( 4 FDA reports)
ABNORMAL FAECES ( 3 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
AXONAL NEUROPATHY ( 3 FDA reports)
BEHCET'S SYNDROME ( 3 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 3 FDA reports)
CATARACT ( 3 FDA reports)
COLECTOMY ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
FALL ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 3 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 3 FDA reports)
HUMAN ANAPLASMOSIS ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INCREASED TENDENCY TO BRUISE ( 3 FDA reports)
INTENTIONAL OVERDOSE ( 3 FDA reports)
INTESTINAL RESECTION ( 3 FDA reports)
INTESTINAL ULCER ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
POSTOPERATIVE ILEUS ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
SALIVARY GLAND ADENOMA ( 3 FDA reports)
SPERM COUNT DECREASED ( 3 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
AMOEBIC COLITIS ( 2 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
BENIGN BREAST NEOPLASM ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
BRONCHITIS VIRAL ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CLUSTER HEADACHE ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COMA ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
DEATH ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEPATIC AMOEBIASIS ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOVITAMINOSIS ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
INADEQUATE ANALGESIA ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
ONYCHOMYCOSIS ( 2 FDA reports)
POOR VENOUS ACCESS ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
SECONDARY HYPOGONADISM ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
SWELLING ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
B-LYMPHOCYTE ABNORMALITIES ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEVICE ADHESION ISSUE ( 1 FDA reports)
DIABETIC ARTHROPATHY ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYELID TUMOUR ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GINGIVAL GRAFT ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NODULE ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PHYLLODES TUMOUR ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
PNEUMONITIS CHEMICAL ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POUCHITIS ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SCAR ( 1 FDA reports)
SEBORRHOEA ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THYROID CYST ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WOUND ( 1 FDA reports)

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