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

ANAEMIA ( 24 FDA reports)
FATIGUE ( 21 FDA reports)
PYREXIA ( 21 FDA reports)
PAIN ( 20 FDA reports)
DYSPNOEA ( 18 FDA reports)
MUSCULAR WEAKNESS ( 17 FDA reports)
SEPSIS ( 17 FDA reports)
INTERSTITIAL LUNG DISEASE ( 16 FDA reports)
PNEUMONIA ( 16 FDA reports)
CHEST PAIN ( 15 FDA reports)
CHEST DISCOMFORT ( 14 FDA reports)
NEUTROPENIA ( 14 FDA reports)
ABDOMINAL PAIN ( 13 FDA reports)
HYPONATRAEMIA ( 13 FDA reports)
RENAL IMPAIRMENT ( 13 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 12 FDA reports)
GASTRITIS ( 12 FDA reports)
HYPOKALAEMIA ( 12 FDA reports)
LEUKOCYTOSIS ( 12 FDA reports)
PARAESTHESIA ( 12 FDA reports)
RECTAL HAEMORRHAGE ( 12 FDA reports)
URINARY TRACT INFECTION ( 12 FDA reports)
ANXIETY ( 11 FDA reports)
ARTHRALGIA ( 11 FDA reports)
ASTHENIA ( 11 FDA reports)
BLOOD GLUCOSE INCREASED ( 11 FDA reports)
COUGH ( 11 FDA reports)
DEEP VEIN THROMBOSIS ( 11 FDA reports)
DIARRHOEA ( 11 FDA reports)
LOBAR PNEUMONIA ( 11 FDA reports)
OSTEOPOROSIS ( 11 FDA reports)
PLEURAL EFFUSION ( 11 FDA reports)
RESPIRATORY DISORDER ( 11 FDA reports)
WEIGHT DECREASED ( 11 FDA reports)
ABDOMINAL PAIN UPPER ( 10 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 10 FDA reports)
CONSTIPATION ( 10 FDA reports)
DEPRESSION ( 10 FDA reports)
DYSURIA ( 10 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 10 FDA reports)
HYPOTENSION ( 10 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 10 FDA reports)
NAUSEA ( 10 FDA reports)
NECK PAIN ( 10 FDA reports)
OEDEMA ( 10 FDA reports)
PALPITATIONS ( 10 FDA reports)
RESPIRATORY DISTRESS ( 10 FDA reports)
ACUTE STRESS DISORDER ( 9 FDA reports)
ANAL INFLAMMATION ( 9 FDA reports)
ANHEDONIA ( 9 FDA reports)
ARTHROPATHY ( 9 FDA reports)
ATELECTASIS ( 9 FDA reports)
BRONCHITIS ( 9 FDA reports)
CERVICAL SPINAL STENOSIS ( 9 FDA reports)
CHOLECYSTITIS ( 9 FDA reports)
CHOLELITHIASIS ( 9 FDA reports)
COLONIC POLYP ( 9 FDA reports)
CONTUSION ( 9 FDA reports)
CYST ( 9 FDA reports)
DERMAL CYST ( 9 FDA reports)
DISABILITY ( 9 FDA reports)
DIVERTICULUM ( 9 FDA reports)
EXOSTOSIS ( 9 FDA reports)
FIBULA FRACTURE ( 9 FDA reports)
FLANK PAIN ( 9 FDA reports)
HAEMORRHOIDS ( 9 FDA reports)
HEPATIC LESION ( 9 FDA reports)
HILAR LYMPHADENOPATHY ( 9 FDA reports)
HYPERLIPIDAEMIA ( 9 FDA reports)
HYPOAESTHESIA ( 9 FDA reports)
INJURY ( 9 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 9 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 9 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 9 FDA reports)
KIDNEY INFECTION ( 9 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 9 FDA reports)
LOCAL SWELLING ( 9 FDA reports)
LUNG NEOPLASM ( 9 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 9 FDA reports)
METASTATIC NEOPLASM ( 9 FDA reports)
MUSCULOSKELETAL PAIN ( 9 FDA reports)
OEDEMA MUCOSAL ( 9 FDA reports)
OSTEOARTHRITIS ( 9 FDA reports)
OSTEONECROSIS OF JAW ( 9 FDA reports)
OSTEOPENIA ( 9 FDA reports)
PAIN IN EXTREMITY ( 9 FDA reports)
PARANASAL SINUS DISCOMFORT ( 9 FDA reports)
PERNICIOUS ANAEMIA ( 9 FDA reports)
PRURITUS ( 9 FDA reports)
PULMONARY FIBROSIS ( 9 FDA reports)
PULMONARY HYPERTENSION ( 9 FDA reports)
RESPIRATORY FAILURE ( 9 FDA reports)
SLEEP APNOEA SYNDROME ( 9 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 9 FDA reports)
THROMBOCYTOSIS ( 9 FDA reports)
TOOTH EXTRACTION ( 9 FDA reports)
VENOUS OCCLUSION ( 9 FDA reports)
VENOUS THROMBOSIS ( 9 FDA reports)
VITAMIN B12 DEFICIENCY ( 9 FDA reports)
VULVOVAGINAL DRYNESS ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 8 FDA reports)
FEELING ABNORMAL ( 8 FDA reports)
HEADACHE ( 8 FDA reports)
INFECTION ( 8 FDA reports)
JOINT SPRAIN ( 8 FDA reports)
NEOPLASM MALIGNANT ( 8 FDA reports)
WHEEZING ( 8 FDA reports)
BLOOD UREA INCREASED ( 7 FDA reports)
BREAST OPERATION ( 7 FDA reports)
BREAST RECONSTRUCTION ( 7 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 7 FDA reports)
EMPHYSEMA ( 7 FDA reports)
FIBROMYALGIA ( 7 FDA reports)
GALLBLADDER OPERATION ( 7 FDA reports)
HEPATIC FAILURE ( 7 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 7 FDA reports)
HYPERSENSITIVITY ( 7 FDA reports)
HYPOPHAGIA ( 7 FDA reports)
MUSCLE STRAIN ( 7 FDA reports)
NEUROPATHY PERIPHERAL ( 7 FDA reports)
OLIGURIA ( 7 FDA reports)
RASH ( 7 FDA reports)
SKIN CYST EXCISION ( 7 FDA reports)
THYROID DISORDER ( 7 FDA reports)
VISUAL ACUITY REDUCED ( 7 FDA reports)
VOMITING ( 7 FDA reports)
ARTERIOSCLEROSIS ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
DRUG ADMINISTRATION ERROR ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
INFLAMMATION ( 6 FDA reports)
INJECTION SITE INDURATION ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
MALAISE ( 6 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
NEPHROGENIC ANAEMIA ( 6 FDA reports)
OSTEOMYELITIS ( 6 FDA reports)
RHABDOMYOLYSIS ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
SHOCK ( 6 FDA reports)
SKIN LACERATION ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 6 FDA reports)
WEIGHT INCREASED ( 6 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
BEDRIDDEN ( 5 FDA reports)
DYSSTASIA ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
HEPATITIS B ( 5 FDA reports)
HYPOGLYCAEMIC COMA ( 5 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
TACHYPNOEA ( 5 FDA reports)
TREMOR ( 5 FDA reports)
ABASIA ( 4 FDA reports)
ACID BASE BALANCE ABNORMAL ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 4 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 4 FDA reports)
BLOOD GASES ABNORMAL ( 4 FDA reports)
BLOOD LACTIC ACID INCREASED ( 4 FDA reports)
BLOOD URIC ACID INCREASED ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
CSF PROTEIN INCREASED ( 4 FDA reports)
EATING DISORDER ( 4 FDA reports)
ELECTROLYTE IMBALANCE ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
LACTIC ACIDOSIS ( 4 FDA reports)
LUNG INFILTRATION ( 4 FDA reports)
MUSCLE ATROPHY ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 4 FDA reports)
MYOPATHY ( 4 FDA reports)
MYOSITIS ( 4 FDA reports)
NEOPLASM ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PERFORMANCE STATUS DECREASED ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
SPINAL OSTEOARTHRITIS ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
ASCITES ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BLOOD AMYLASE INCREASED ( 3 FDA reports)
BRONCHIOLITIS ( 3 FDA reports)
BRONCHOSTENOSIS ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CAECITIS ( 3 FDA reports)
CALCULUS BLADDER ( 3 FDA reports)
CAPILLARY LEAK SYNDROME ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
ENGRAFT FAILURE ( 3 FDA reports)
EROSIVE OESOPHAGITIS ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HEPATIC CIRRHOSIS ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HYPERTENSIVE CRISIS ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 3 FDA reports)
OBESITY ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PULMONARY HAEMORRHAGE ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
RETINAL VEIN OCCLUSION ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
VITREOUS FLOATERS ( 3 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AGITATION ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CARDIAC ANEURYSM ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHILLS ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 2 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 2 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG PHYSIOLOGIC INCOMPATIBILITY ( 2 FDA reports)
DRUG-INDUCED LIVER INJURY ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
FALL ( 2 FDA reports)
FIBROMA ( 2 FDA reports)
FOLLICULITIS ( 2 FDA reports)
FUNGAL PERITONITIS ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 2 FDA reports)
HEPATITIS B DNA INCREASED ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INTUSSUSCEPTION ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MOUTH CYST ( 2 FDA reports)
MUSCLE INJURY ( 2 FDA reports)
NASOGASTRIC OUTPUT HIGH ( 2 FDA reports)
NEOPLASM PROGRESSION ( 2 FDA reports)
NERVE ROOT INJURY CERVICAL ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OPPORTUNISTIC INFECTION ( 2 FDA reports)
OSTEOMYELITIS ACUTE ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PROCTITIS ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
SHUNT OCCLUSION ( 2 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL WALL INFECTION ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMINO ACID LEVEL DECREASED ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE LESION ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BULIMIA NERVOSA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMA ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GLOSSOPHARYNGEAL NERVE PARALYSIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MARASMUS ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEUROBLASTOMA ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERITONEAL ABSCESS ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
POLYP ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
REACTION TO PRESERVATIVES ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
XITH NERVE PARALYSIS ( 1 FDA reports)

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