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

RENAL FAILURE ( 19 FDA reports)
LIP SWELLING ( 18 FDA reports)
MYALGIA ( 17 FDA reports)
SWOLLEN TONGUE ( 17 FDA reports)
BULBAR PALSY ( 15 FDA reports)
AGEUSIA ( 13 FDA reports)
ANOSMIA ( 13 FDA reports)
DRY EYE ( 13 FDA reports)
GLOSSODYNIA ( 13 FDA reports)
PLEURAL EFFUSION ( 13 FDA reports)
SPEECH DISORDER ( 13 FDA reports)
DYSPHAGIA ( 12 FDA reports)
INSOMNIA ( 12 FDA reports)
OROPHARYNGEAL BLISTERING ( 12 FDA reports)
STRESS ( 12 FDA reports)
ORAL PAIN ( 11 FDA reports)
CHEILITIS ( 10 FDA reports)
EYE PRURITUS ( 9 FDA reports)
DIPLOPIA ( 8 FDA reports)
LIP DISORDER ( 8 FDA reports)
PAIN IN EXTREMITY ( 8 FDA reports)
TONGUE BLISTERING ( 8 FDA reports)
LUNG ADENOCARCINOMA ( 7 FDA reports)
DIARRHOEA ( 6 FDA reports)
DISEASE PROGRESSION ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
LUNG NEOPLASM MALIGNANT ( 6 FDA reports)
SWELLING FACE ( 6 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 5 FDA reports)
HETEROPHORIA ( 5 FDA reports)
INTENTIONAL OVERDOSE ( 5 FDA reports)
RASH ( 5 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SKIN FISSURES ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
CORONARY ARTERY THROMBOSIS ( 3 FDA reports)
COUGH ( 3 FDA reports)
DIVERTICULUM ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DRUG INTOLERANCE ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
FALL ( 3 FDA reports)
GALLBLADDER ENLARGEMENT ( 3 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HIP ARTHROPLASTY ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
INGUINAL HERNIA ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 3 FDA reports)
LEFT ATRIAL DILATATION ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
MICTURITION URGENCY ( 3 FDA reports)
MITRAL VALVE DISEASE ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MOOD SWINGS ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
PANCREATIC ATROPHY ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
POLYNEUROPATHY ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 3 FDA reports)
RENAL ATROPHY ( 3 FDA reports)
RIGHT ATRIAL DILATATION ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
URINARY HESITATION ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VASCULITIC RASH ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GOUT ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
MACULAR OEDEMA ( 2 FDA reports)
MANIA ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PITTING OEDEMA ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RENAL AGENESIS ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
RENAL VEIN THROMBOSIS ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
SOCIAL PROBLEM ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
URINE COLOUR ABNORMAL ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INHIBITOR FOETOPATHY ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APHONIA ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
CONGENITAL BLADDER ANOMALY ( 1 FDA reports)
CONGENITAL FOOT MALFORMATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DELAYED FONTANELLE CLOSURE ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSPRAXIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
MOTOR NEURONE DISEASE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEONATAL ASPHYXIA ( 1 FDA reports)
NEONATAL HYPOTENSION ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHOTOSENSITIVE RASH ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL CORTICAL NECROSIS ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL FAILURE NEONATAL ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SKULL MALFORMATION ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UTERINE SPASM ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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