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

DYSPNOEA ( 13 FDA reports)
PNEUMONIA ( 12 FDA reports)
RESPIRATORY TRACT INFECTION ( 10 FDA reports)
SEPSIS ( 10 FDA reports)
DERMATITIS ALLERGIC ( 9 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 9 FDA reports)
DRUG INEFFECTIVE ( 9 FDA reports)
PYREXIA ( 9 FDA reports)
BREAST CANCER ( 8 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 8 FDA reports)
CIRCULATORY COLLAPSE ( 8 FDA reports)
COLITIS ULCERATIVE ( 8 FDA reports)
INFUSION RELATED REACTION ( 8 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
ANAEMIA ( 7 FDA reports)
DEATH ( 7 FDA reports)
HYPOTENSION ( 7 FDA reports)
ISCHAEMIC STROKE ( 7 FDA reports)
URINARY TRACT INFECTION ( 7 FDA reports)
APLASIA PURE RED CELL ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
OSTEOPOROSIS ( 6 FDA reports)
SYNOVITIS ( 6 FDA reports)
TUBERCULOSIS ( 6 FDA reports)
ABORTION SPONTANEOUS ( 5 FDA reports)
BASAL CELL CARCINOMA ( 5 FDA reports)
DRUG ERUPTION ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HEMIPARESIS ( 5 FDA reports)
LATENT TUBERCULOSIS ( 5 FDA reports)
MUSCULOSKELETAL PAIN ( 5 FDA reports)
OSTEOARTHRITIS ( 5 FDA reports)
OSTEONECROSIS ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
PSORIASIS ( 5 FDA reports)
RASH ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
TUBERCULIN TEST POSITIVE ( 5 FDA reports)
ANAL ABSCESS ( 4 FDA reports)
ARTHRITIS ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BORRELIA INFECTION ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
CARDIOPULMONARY FAILURE ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 4 FDA reports)
COUGH ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 4 FDA reports)
GROIN ABSCESS ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
MYELODYSPLASTIC SYNDROME ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
OVARIAN NEOPLASM ( 4 FDA reports)
PAIN ( 4 FDA reports)
PREGNANCY ( 4 FDA reports)
PYELONEPHRITIS CHRONIC ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 4 FDA reports)
RENAL CYST ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
ABSCESS JAW ( 3 FDA reports)
ACTINIC KERATOSIS ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
BRAIN ABSCESS ( 3 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DYSLOGIA ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 3 FDA reports)
GALLBLADDER POLYP ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HEPATIC NEOPLASM ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HODGKIN'S DISEASE ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
METASTASES TO BONE ( 3 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
METASTASES TO KIDNEY ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
NASAL SEPTUM DEVIATION ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
NEONATAL ASPIRATION ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
OTITIS MEDIA CHRONIC ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PERIARTHRITIS ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
PYELONEPHRITIS ACUTE ( 3 FDA reports)
RALES ( 3 FDA reports)
RASH PUSTULAR ( 3 FDA reports)
SARCOIDOSIS ( 3 FDA reports)
SKIN CANCER ( 3 FDA reports)
SKIN FISSURES ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
TONSILLAR HYPERTROPHY ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
TREMOR ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
ABSCESS SOFT TISSUE ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ARTHRITIS BACTERIAL ( 2 FDA reports)
ARTHROPOD STING ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BREAST ABSCESS ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CHRONIC SINUSITIS ( 2 FDA reports)
CYST ( 2 FDA reports)
DIABETIC GANGRENE ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DUODENOGASTRIC REFLUX ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
GASTROENTERITIS PROTEUS ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
INDUCED LABOUR ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LEUKOENCEPHALOMYELITIS ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LUMBAR SPINAL STENOSIS ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MASTITIS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OSTEOMYELITIS CHRONIC ( 2 FDA reports)
OSTEOPOROTIC FRACTURE ( 2 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
RADICULAR SYNDROME ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
SALMONELLOSIS ( 2 FDA reports)
SCAR ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STRESS ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
THROMBIN TIME PROLONGED ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
AORTIC INJURY ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 1 FDA reports)
ARTHRITIS SALMONELLA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLESTATIC LIVER INJURY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
CONGENITAL MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
CONGENITAL NAEVUS ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GRIP STRENGTH ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HIGH RISK PREGNANCY ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MASS ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL HYPERAEMIA ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
NASAL NEOPLASM ( 1 FDA reports)
NASAL NEOPLASM BENIGN ( 1 FDA reports)
NASOPHARYNGEAL NEOPLASM BENIGN ( 1 FDA reports)
NEONATAL ASPHYXIA ( 1 FDA reports)
NEONATAL INFECTION ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NERVE BLOCK ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVARIAN HYPERSTIMULATION SYNDROME ( 1 FDA reports)
OVARIAN MASS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PERIARTICULAR DISORDER ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIPROCTITIS ( 1 FDA reports)
PERITONEAL CARCINOMA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
POLYHYDRAMNIOS ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 1 FDA reports)
PREGNANCY ON CONTRACEPTIVE ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROLONGED LABOUR ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PURULENT SYNOVITIS ( 1 FDA reports)
RENAL ADENOMA ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SHUNT MALFUNCTION ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STAG HORN CALCULUS ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUPERNUMERARY NIPPLE ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNOVECTOMY ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
ULTRASOUND UTERUS ABNORMAL ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENOUS STENOSIS ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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