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

ANXIETY ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
DEPRESSION ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
PAIN ( 3 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
APATHY ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLADDER IRRITATION ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BURN INFECTION ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
DEATH OF FRIEND ( 1 FDA reports)
DEATH OF PARENT ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
FALL ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MANIA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIODONTAL DISEASE ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)

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