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GENERAL PHYSICAL HEALTH DETERIORATION ( 25 FDA reports)
PNEUMONIA ( 22 FDA reports)
CYTOLYTIC HEPATITIS ( 21 FDA reports)
DECREASED APPETITE ( 19 FDA reports)
DRUG INTERACTION ( 18 FDA reports)
ASTHENIA ( 17 FDA reports)
PYREXIA ( 17 FDA reports)
DEATH ( 15 FDA reports)
THROMBOCYTOPENIA ( 15 FDA reports)
ARTHRALGIA ( 14 FDA reports)
OSTEONECROSIS ( 14 FDA reports)
VOMITING ( 14 FDA reports)
INFECTION ( 13 FDA reports)
RENAL FAILURE ( 13 FDA reports)
BACK PAIN ( 12 FDA reports)
CHOLESTASIS ( 12 FDA reports)
PULMONARY EMBOLISM ( 11 FDA reports)
RENAL FAILURE ACUTE ( 11 FDA reports)
FALL ( 10 FDA reports)
FATIGUE ( 10 FDA reports)
PAIN IN EXTREMITY ( 10 FDA reports)
DYSPNOEA ( 9 FDA reports)
HEPATIC ENCEPHALOPATHY ( 9 FDA reports)
HEPATITIS FULMINANT ( 9 FDA reports)
OEDEMA PERIPHERAL ( 9 FDA reports)
PAIN ( 9 FDA reports)
TACHYCARDIA ( 9 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 8 FDA reports)
DIZZINESS ( 8 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 8 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 8 FDA reports)
HEPATITIS ( 8 FDA reports)
MENINGIOMA ( 8 FDA reports)
SOMNOLENCE ( 8 FDA reports)
SYNCOPE ( 8 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
BLEEDING ANOVULATORY ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
COUGH ( 7 FDA reports)
ECCHYMOSIS ( 7 FDA reports)
MALAISE ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
PURPURA ( 7 FDA reports)
RHABDOMYOLYSIS ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
COMA ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
RECTAL HAEMORRHAGE ( 6 FDA reports)
WEIGHT INCREASED ( 6 FDA reports)
AGRANULOCYTOSIS ( 5 FDA reports)
ANAEMIA ( 5 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
HEPATITIS CHOLESTATIC ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
LEUKOCYTOSIS ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
OESOPHAGITIS ( 5 FDA reports)
PROSTATE CANCER ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
AGGRESSION ( 4 FDA reports)
APATHY ( 4 FDA reports)
BLINDNESS ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HEPATOCELLULAR INJURY ( 4 FDA reports)
HIP FRACTURE ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
JAUNDICE CHOLESTATIC ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
MUSCLE RIGIDITY ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
TOOTH EXTRACTION ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
AUTOIMMUNE HEPATITIS ( 3 FDA reports)
BONE DEBRIDEMENT ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
FEEDING DISORDER ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FISTULA ( 3 FDA reports)
FOOT FRACTURE ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATOCELLULAR DAMAGE ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
INTERMITTENT CLAUDICATION ( 3 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
ORAL DISORDER ( 3 FDA reports)
OSTEOLYSIS ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
PAIN IN JAW ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PHLEBITIS ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PRIMARY SEQUESTRUM ( 3 FDA reports)
PROSTATE CANCER METASTATIC ( 3 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 3 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
SCIATICA ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
WEIGHT BEARING DIFFICULTY ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACTINOMYCOSIS ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASEPTIC NECROSIS BONE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BONE DENSITY DECREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIAC PACEMAKER INSERTION ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CSF PROTEIN INCREASED ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
ESCHAR ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
FEBRILE BONE MARROW APLASIA ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GINGIVAL INFECTION ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMOCHROMATOSIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOPROTHROMBINAEMIA ( 2 FDA reports)
HYPOREFLEXIA ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
IRIDOCYCLITIS ( 2 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JAW DISORDER ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MENINGEOMAS SURGERY ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NEUTROPHILIA ( 2 FDA reports)
OBSTRUCTIVE UROPATHY ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
OSTEONECROSIS OF JAW ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PARAPLEGIA ( 2 FDA reports)
PITUITARY HAEMORRHAGE ( 2 FDA reports)
PITUITARY TUMOUR ( 2 FDA reports)
PITUITARY TUMOUR BENIGN ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RETCHING ( 2 FDA reports)
SCROTAL HAEMATOMA ( 2 FDA reports)
SCROTAL IRRITATION ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SOPOR ( 2 FDA reports)
SPINAL CORD COMPRESSION ( 2 FDA reports)
SPINAL CORD INJURY CERVICAL ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SWELLING ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TRANSFERRIN DECREASED ( 2 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 2 FDA reports)
TREMOR ( 2 FDA reports)
TUMOUR EMBOLISM ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WALKING DISABILITY ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALCOHOL INTOLERANCE ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANION GAP ABNORMAL ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLIGHTED OVUM ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BONE FISTULA ( 1 FDA reports)
BONE LESION ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BONE TRIMMING ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRONCHOPULMONARY DISEASE ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COR PULMONALE ACUTE ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CRYING ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSGLOBULINAEMIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EPISCLERITIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GINGIVAL OPERATION ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFUSION SITE NECROSIS ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL ABNORMAL ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JAW OPERATION ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORAL SURGERY ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POST CONCUSSION SYNDROME ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
PROSTHESIS USER ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RENAL AGENESIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOLITARY KIDNEY ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STOMATITIS NECROTISING ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SURGERY ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOOTH REPAIR ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
URETHRAL OBSTRUCTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
XEROPHTHALMIA ( 1 FDA reports)

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