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

PAIN ( 23 FDA reports)
PNEUMONIA ( 23 FDA reports)
ASTHENIA ( 22 FDA reports)
FALL ( 22 FDA reports)
FATIGUE ( 21 FDA reports)
DIZZINESS ( 18 FDA reports)
FEMUR FRACTURE ( 16 FDA reports)
OEDEMA PERIPHERAL ( 16 FDA reports)
ARTHRALGIA ( 15 FDA reports)
NAUSEA ( 15 FDA reports)
PAIN IN EXTREMITY ( 15 FDA reports)
DYSPNOEA ( 14 FDA reports)
MALAISE ( 14 FDA reports)
VOMITING ( 14 FDA reports)
COUGH ( 11 FDA reports)
HEADACHE ( 11 FDA reports)
DEHYDRATION ( 10 FDA reports)
DRUG INEFFECTIVE ( 10 FDA reports)
PRURITUS ( 10 FDA reports)
TREMOR ( 10 FDA reports)
ATRIAL FIBRILLATION ( 9 FDA reports)
BACK PAIN ( 9 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 9 FDA reports)
HYPERTENSION ( 9 FDA reports)
PYREXIA ( 9 FDA reports)
BLOOD PRESSURE INCREASED ( 8 FDA reports)
HYPOTENSION ( 8 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 8 FDA reports)
PULMONARY EMBOLISM ( 8 FDA reports)
WEIGHT DECREASED ( 8 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 7 FDA reports)
CHEST PAIN ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
DEATH ( 7 FDA reports)
DIARRHOEA ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
OSTEOMYELITIS ( 7 FDA reports)
RENAL FAILURE ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
ABASIA ( 6 FDA reports)
DECREASED APPETITE ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
DRY MOUTH ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
OESOPHAGEAL ULCER ( 6 FDA reports)
PARAESTHESIA ( 6 FDA reports)
RASH ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
ABSCESS ( 5 FDA reports)
ALOPECIA ( 5 FDA reports)
ANAEMIA ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
BLOOD SODIUM DECREASED ( 5 FDA reports)
FLANK PAIN ( 5 FDA reports)
GASTRITIS ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
INFUSION RELATED REACTION ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
RECTAL HAEMORRHAGE ( 5 FDA reports)
REFLUX OESOPHAGITIS ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
DYSSTASIA ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
IRRITABLE BOWEL SYNDROME ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
MENTAL STATUS CHANGES ( 4 FDA reports)
MOBILITY DECREASED ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
NEOPLASM MALIGNANT ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
PULMONARY FIBROSIS ( 4 FDA reports)
RHEUMATOID ARTHRITIS ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ALBUMIN URINE PRESENT ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANHEDONIA ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD CREATINE INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BONE DENSITY DECREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
DEFORMITY ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
ECONOMIC PROBLEM ( 3 FDA reports)
FISTULA ( 3 FDA reports)
FLUID INTAKE REDUCED ( 3 FDA reports)
FOOT FRACTURE ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SKIN HYPERTROPHY ( 3 FDA reports)
SKIN INDURATION ( 3 FDA reports)
SKIN LESION ( 3 FDA reports)
STRESS FRACTURE ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
THIRST ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
URINARY TRACT DISORDER ( 3 FDA reports)
URINE ANALYSIS ABNORMAL ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ARTHRODESIS ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BONE FISTULA ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COMA ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CYSTOID MACULAR OEDEMA ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
EXTREMITY CONTRACTURE ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FRACTURE DISPLACEMENT ( 2 FDA reports)
FUNGAL OESOPHAGITIS ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
HAEMANGIOMA OF LIVER ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HERPES ZOSTER DISSEMINATED ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HUNGER ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
INCORRECT STORAGE OF DRUG ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTESTINAL RESECTION ( 2 FDA reports)
JOINT CONTRACTURE ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIFE SUPPORT ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
METATARSALGIA ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MUSCULAR DYSTROPHY ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OESOPHAGEAL INJURY ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OSTEONECROSIS OF JAW ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PLEOCYTOSIS ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POLYARTHRITIS ( 2 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 2 FDA reports)
POST HERPETIC NEURALGIA ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PULMONARY TUBERCULOSIS ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH PAPULOSQUAMOUS ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SEROCONVERSION TEST POSITIVE ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
TOXOPLASMOSIS ( 2 FDA reports)
TRISMUS ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
VASCULITIS CEREBRAL ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALLERGIC COUGH ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ALVEOLITIS FIBROSING ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE FORMATION DECREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CARCINOMA IN SITU OF SKIN ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CLITORAL ENGORGEMENT ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECREASED INSULIN REQUIREMENT ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIFFUSE AXONAL INJURY ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENLARGED CLITORIS ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EPITHELIOID SARCOMA ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EYE ALLERGY ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL DISCHARGE ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERTROPHIC OBSTRUCTIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMMUNOGLOBULINS INCREASED ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INBORN ERROR OF METABOLISM ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEISSERIA INFECTION ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NODULE ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOMA ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVARIAN CYST RUPTURED ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PSEUDOPHAEOCHROMOCYTOMA ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PUTAMEN HAEMORRHAGE ( 1 FDA reports)
RADIATION SICKNESS SYNDROME ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNOVIAL DISORDER ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRIGEMINAL NERVE DISORDER ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
YAWNING ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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