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

DEPRESSION ( 21 FDA reports)
FATIGUE ( 12 FDA reports)
DYSPNOEA ( 11 FDA reports)
INSOMNIA ( 11 FDA reports)
CONFUSIONAL STATE ( 10 FDA reports)
FEELING ABNORMAL ( 10 FDA reports)
SOMNOLENCE ( 10 FDA reports)
DIZZINESS ( 9 FDA reports)
DIARRHOEA ( 8 FDA reports)
FALL ( 8 FDA reports)
HYPERTENSION ( 8 FDA reports)
OVERDOSE ( 8 FDA reports)
SUICIDAL IDEATION ( 8 FDA reports)
WEIGHT INCREASED ( 8 FDA reports)
ANXIETY ( 7 FDA reports)
ASTHENIA ( 7 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
HEART RATE INCREASED ( 7 FDA reports)
MANIA ( 7 FDA reports)
PAIN ( 7 FDA reports)
TREATMENT NONCOMPLIANCE ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
ANGER ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
MALAISE ( 6 FDA reports)
SUICIDE ATTEMPT ( 6 FDA reports)
TREMOR ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
BLOOD MAGNESIUM DECREASED ( 5 FDA reports)
BLOOD POTASSIUM DECREASED ( 5 FDA reports)
CONVERSION DISORDER ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
DYSPHONIA ( 5 FDA reports)
EPISTAXIS ( 5 FDA reports)
HAEMOPTYSIS ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
NEUROPATHY PERIPHERAL ( 5 FDA reports)
PHARYNGEAL MASS ( 5 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 5 FDA reports)
THYROID DISORDER ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 5 FDA reports)
ABASIA ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
DRUG ADMINISTRATION ERROR ( 4 FDA reports)
EXPIRED DRUG ADMINISTERED ( 4 FDA reports)
FLANK PAIN ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
INCREASED APPETITE ( 4 FDA reports)
INGUINAL HERNIA ( 4 FDA reports)
INITIAL INSOMNIA ( 4 FDA reports)
INJECTION SITE SWELLING ( 4 FDA reports)
IRRITABILITY ( 4 FDA reports)
JUDGEMENT IMPAIRED ( 4 FDA reports)
LIPOMA ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
RASH ( 4 FDA reports)
SMOKER ( 4 FDA reports)
TESTICULAR SWELLING ( 4 FDA reports)
THINKING ABNORMAL ( 4 FDA reports)
VIRAL LOAD INCREASED ( 4 FDA reports)
BACK PAIN ( 3 FDA reports)
BLADDER CANCER ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
CRYING ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
EOSINOPHIL COUNT DECREASED ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HYPOMANIA ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MENORRHAGIA ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
ORAL HERPES ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PHOTOPHOBIA ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ADRENAL MASS ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
BEREAVEMENT REACTION ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CONGENITAL TRICUSPID VALVE STENOSIS ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FOOD CRAVING ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOPLASTIC RIGHT HEART SYNDROME ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PITUITARY TUMOUR ( 2 FDA reports)
PITUITARY TUMOUR BENIGN ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SEPTIC EMBOLUS ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SOCIAL PROBLEM ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABORTION ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EAR LOBE INFECTION ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOGONADISM MALE ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL CYST ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL LICHEN PLANUS ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCAB ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VARICOSE ULCERATION ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use