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

NAUSEA ( 9 FDA reports)
VOMITING ( 8 FDA reports)
CHILLS ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
ADHESION ( 5 FDA reports)
ADVERSE EVENT ( 5 FDA reports)
AEROPHAGIA ( 5 FDA reports)
ANAPHYLACTIC REACTION ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
BREAST PAIN ( 5 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
DRUG HYPERSENSITIVITY ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
DRUG INTOLERANCE ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
DYSURIA ( 5 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 5 FDA reports)
GLOSSODYNIA ( 5 FDA reports)
HELICOBACTER INFECTION ( 5 FDA reports)
HOT FLUSH ( 5 FDA reports)
LIMB INJURY ( 5 FDA reports)
LIPOMATOSIS ( 5 FDA reports)
LYMPHADENOPATHY ( 5 FDA reports)
MALAISE ( 5 FDA reports)
MICROCYTIC ANAEMIA ( 5 FDA reports)
MIGRAINE ( 5 FDA reports)
NASAL CONGESTION ( 5 FDA reports)
NEUROPATHY PERIPHERAL ( 5 FDA reports)
ODYNOPHAGIA ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 5 FDA reports)
OESOPHAGITIS ULCERATIVE ( 5 FDA reports)
ORAL CANDIDIASIS ( 5 FDA reports)
PAIN ( 5 FDA reports)
PANCREATIC INSUFFICIENCY ( 5 FDA reports)
PHOTOSENSITIVITY REACTION ( 5 FDA reports)
RHEUMATOID ARTHRITIS ( 5 FDA reports)
SINUSITIS ( 5 FDA reports)
SJOGREN'S SYNDROME ( 5 FDA reports)
SUBCUTANEOUS NODULE ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
THIRST ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
URETHRAL DISORDER ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
VAGINAL DISCHARGE ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
NASAL SEPTUM DEVIATION ( 4 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
STRESS ( 4 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 4 FDA reports)
ANXIETY ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
COUGH ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DEVICE RELATED SEPSIS ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HYPERCHLORHYDRIA ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
MULTIPLE ALLERGIES ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
URINE FLOW DECREASED ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FAMILY STRESS ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
INJURY ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
LIPIDS ABNORMAL ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CYST ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTESTINAL ADHESION LYSIS ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 1 FDA reports)
MYOFASCIAL SPASM ( 1 FDA reports)
NASAL POLYPECTOMY ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SICCA SYNDROME ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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