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

INJECTION SITE PAIN ( 10 FDA reports)
HEADACHE ( 7 FDA reports)
MIGRAINE ( 7 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
CONVULSION ( 5 FDA reports)
SINUSITIS ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
INJECTION SITE ERYTHEMA ( 4 FDA reports)
INJECTION SITE HAEMORRHAGE ( 4 FDA reports)
INJECTION SITE IRRITATION ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
THROAT IRRITATION ( 4 FDA reports)
BRAIN NEOPLASM ( 3 FDA reports)
CHRONIC SINUSITIS ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
INJECTION SITE NODULE ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
PAIN ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
STRESS ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
COUGH ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
ENDOMETRIOSIS ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INJECTION SITE BURNING ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INJECTION SITE STINGING ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENISCUS LESION ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SKIN TIGHTNESS ( 2 FDA reports)
TREMOR ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NODULE ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STENOTROPHOMONAS SEPSIS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VITAMIN D ABNORMAL ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WHITE CLOT SYNDROME ( 1 FDA reports)

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