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

NAUSEA ( 48 FDA reports)
FATIGUE ( 47 FDA reports)
ASTHENIA ( 40 FDA reports)
DIARRHOEA ( 40 FDA reports)
PAIN IN EXTREMITY ( 39 FDA reports)
MALAISE ( 37 FDA reports)
GAIT DISTURBANCE ( 36 FDA reports)
VOMITING ( 36 FDA reports)
ANAEMIA ( 32 FDA reports)
BLOOD PRESSURE INCREASED ( 28 FDA reports)
DYSPNOEA ( 27 FDA reports)
ABDOMINAL PAIN ( 25 FDA reports)
FALL ( 25 FDA reports)
MYALGIA ( 25 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 23 FDA reports)
MUSCULAR WEAKNESS ( 23 FDA reports)
ARTHRALGIA ( 22 FDA reports)
INJECTION SITE PAIN ( 22 FDA reports)
CEREBROVASCULAR ACCIDENT ( 21 FDA reports)
FEELING ABNORMAL ( 21 FDA reports)
HEADACHE ( 21 FDA reports)
MEMORY IMPAIRMENT ( 21 FDA reports)
DIZZINESS ( 20 FDA reports)
LOSS OF CONSCIOUSNESS ( 20 FDA reports)
PNEUMONIA ( 20 FDA reports)
DEATH ( 19 FDA reports)
EPISTAXIS ( 19 FDA reports)
HYPOTENSION ( 19 FDA reports)
INFLUENZA ( 18 FDA reports)
STRESS ( 17 FDA reports)
BLOOD PRESSURE DECREASED ( 16 FDA reports)
CARDIAC DISORDER ( 16 FDA reports)
OEDEMA PERIPHERAL ( 16 FDA reports)
PEDAL PULSE ABNORMAL ( 16 FDA reports)
SPEECH DISORDER ( 16 FDA reports)
VISUAL FIELD DEFECT ( 16 FDA reports)
HYPOPHAGIA ( 15 FDA reports)
PAIN ( 15 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 15 FDA reports)
WEIGHT DECREASED ( 15 FDA reports)
CHEST PAIN ( 14 FDA reports)
CHILLS ( 13 FDA reports)
MUSCULOSKELETAL PAIN ( 13 FDA reports)
PYREXIA ( 13 FDA reports)
VISION BLURRED ( 13 FDA reports)
BONE PAIN ( 12 FDA reports)
DECREASED APPETITE ( 12 FDA reports)
HYPERTENSION ( 12 FDA reports)
MYOCARDIAL INFARCTION ( 12 FDA reports)
ANGINA PECTORIS ( 11 FDA reports)
BLOOD SODIUM DECREASED ( 11 FDA reports)
DRUG INTERACTION ( 11 FDA reports)
ABASIA ( 10 FDA reports)
CONFUSIONAL STATE ( 10 FDA reports)
ANXIETY ( 9 FDA reports)
DEPRESSION ( 9 FDA reports)
HYPERGLYCAEMIA ( 9 FDA reports)
PRODUCTIVE COUGH ( 9 FDA reports)
PRURITUS ( 9 FDA reports)
BACK PAIN ( 8 FDA reports)
BALANCE DISORDER ( 8 FDA reports)
BRONCHITIS ( 8 FDA reports)
CARBON MONOXIDE POISONING ( 8 FDA reports)
CONSTIPATION ( 8 FDA reports)
DYSPEPSIA ( 8 FDA reports)
FACE OEDEMA ( 8 FDA reports)
HYPERSENSITIVITY ( 8 FDA reports)
PALPITATIONS ( 8 FDA reports)
PSORIASIS ( 8 FDA reports)
WEIGHT INCREASED ( 8 FDA reports)
ANOREXIA ( 7 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
COUGH ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
NEOPLASM MALIGNANT ( 7 FDA reports)
OROPHARYNGEAL PAIN ( 7 FDA reports)
RASH ( 7 FDA reports)
SOMNOLENCE ( 7 FDA reports)
TACHYCARDIA ( 7 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
ANAPHYLACTIC REACTION ( 6 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
ASTHMA ( 6 FDA reports)
CHOLECYSTITIS ACUTE ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 6 FDA reports)
HEART RATE INCREASED ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
ILL-DEFINED DISORDER ( 6 FDA reports)
NASOPHARYNGITIS ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
SPUTUM DISCOLOURED ( 6 FDA reports)
TREMOR ( 6 FDA reports)
AGGRESSION ( 5 FDA reports)
AMNESIA ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
CARDIOMYOPATHY ( 5 FDA reports)
CATARACT OPERATION ( 5 FDA reports)
COLON CANCER ( 5 FDA reports)
CORONARY ARTERY OCCLUSION ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
HEART RATE DECREASED ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
INFUSION RELATED REACTION ( 5 FDA reports)
ISCHAEMIC STROKE ( 5 FDA reports)
NEPHROLITHIASIS ( 5 FDA reports)
ORTHOSTATIC HYPOTENSION ( 5 FDA reports)
OXYGEN SATURATION DECREASED ( 5 FDA reports)
PRESYNCOPE ( 5 FDA reports)
PSYCHIATRIC SYMPTOM ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
RIB FRACTURE ( 5 FDA reports)
SWELLING ( 5 FDA reports)
SWELLING FACE ( 5 FDA reports)
THROAT IRRITATION ( 5 FDA reports)
THROMBOPHLEBITIS ( 5 FDA reports)
URINARY TRACT OBSTRUCTION ( 5 FDA reports)
ABDOMINAL MASS ( 4 FDA reports)
ABNORMAL FAECES ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 4 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
ARTHRITIS ( 4 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BRONCHOSPASM ( 4 FDA reports)
BURSITIS ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
DECREASED INTEREST ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
INFECTION ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
MELAENA ( 4 FDA reports)
MOBILITY DECREASED ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
NECK PAIN ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
OESOPHAGITIS ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PELVIC FRACTURE ( 4 FDA reports)
PLANTAR FASCIITIS ( 4 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
VERTIGO POSITIONAL ( 4 FDA reports)
ABDOMINAL INFECTION ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ANGER ( 3 FDA reports)
ARTHROPATHY ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
BILIARY COLIC ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 3 FDA reports)
BONE DENSITY DECREASED ( 3 FDA reports)
BREAST MASS ( 3 FDA reports)
COMA ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CORONARY ARTERY THROMBOSIS ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
EJACULATION FAILURE ( 3 FDA reports)
EYE INFECTION ( 3 FDA reports)
FACIAL PALSY ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
HYPOKINESIA ( 3 FDA reports)
INJURY ( 3 FDA reports)
LIMB INJURY ( 3 FDA reports)
MENISCUS LESION ( 3 FDA reports)
MOUTH ULCERATION ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
NAIL DISCOLOURATION ( 3 FDA reports)
NIGHTMARE ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OPEN WOUND ( 3 FDA reports)
PALLIATIVE CARE ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PERICARDITIS ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
PROSTATE CANCER METASTATIC ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SKULL FRACTURE ( 3 FDA reports)
SNEEZING ( 3 FDA reports)
SURGERY ( 3 FDA reports)
TONGUE OEDEMA ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
APALLIC SYNDROME ( 2 FDA reports)
ASOCIAL BEHAVIOUR ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BLOOD OSMOLARITY DECREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARBOHYDRATE METABOLISM DISORDER ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIABETIC COMA ( 2 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GASTRIC HYPOMOTILITY ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GINGIVAL PAIN ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MALABSORPTION ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NECK MASS ( 2 FDA reports)
NEGATIVE THOUGHTS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
RALES ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY RATE ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SKIN CANCER ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
SYNOVITIS ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPLICATION SITE HAEMATOMA ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
FEMALE REPRODUCTIVE NEOPLASM ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INVESTIGATION ( 1 FDA reports)
IRIS ATROPHY ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG NEOPLASM SURGERY ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RETINAL CYST ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
THALASSAEMIA ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
VAGINAL INFLAMMATION ( 1 FDA reports)
VARICOSE VEIN RUPTURED ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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