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

DRUG INEFFECTIVE ( 14 FDA reports)
FATIGUE ( 12 FDA reports)
PAIN ( 11 FDA reports)
HEADACHE ( 10 FDA reports)
MULTIPLE DRUG OVERDOSE ( 10 FDA reports)
DEPRESSION ( 8 FDA reports)
DIZZINESS ( 8 FDA reports)
FEELING ABNORMAL ( 8 FDA reports)
FALL ( 7 FDA reports)
AMNESIA ( 6 FDA reports)
ARTHRALGIA ( 6 FDA reports)
ASTHENIA ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
SUICIDAL IDEATION ( 6 FDA reports)
THERAPY NON-RESPONDER ( 6 FDA reports)
VISION BLURRED ( 6 FDA reports)
WEIGHT DECREASED ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
NERVOUSNESS ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
RHABDOMYOLYSIS ( 5 FDA reports)
ROAD TRAFFIC ACCIDENT ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
VISUAL DISTURBANCE ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
CHEST PAIN ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DRUG EFFECT DECREASED ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HEAD INJURY ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
ABASIA ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ALCOHOL USE ( 3 FDA reports)
ANGER ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
BABESIOSIS ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHILLS ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
EYELID PTOSIS ( 3 FDA reports)
IMPULSE-CONTROL DISORDER ( 3 FDA reports)
JOINT DISLOCATION ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
LYME DISEASE ( 3 FDA reports)
MOOD SWINGS ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SPINAL DISORDER ( 3 FDA reports)
TREMOR ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
AGGRESSION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
BACK INJURY ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONGENITAL MEGAURETER ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CRYING ( 2 FDA reports)
CYANOPSIA ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FALLOPIAN TUBE DISORDER ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
HAND FRACTURE ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INJURY ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
KNEE OPERATION ( 2 FDA reports)
MENSTRUAL DISORDER ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
SCROTAL SWELLING ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SURGERY ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
UTERINE ATONY ( 2 FDA reports)
UTERINE DISORDER ( 2 FDA reports)
UTERINE HAEMORRHAGE ( 2 FDA reports)
UTERINE POLYP ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BITE ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BREAST COSMETIC SURGERY ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BUNION ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CATAPLEXY ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CLONUS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLON POLYPECTOMY ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DENTURE WEARER ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EAR INJURY ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOMETRIAL HYPOPLASIA ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXCESSIVE EXERCISE ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HIP SWELLING ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LIGAMENT INJURY ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MASS ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERITONEAL TUBERCULOSIS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POSTOPERATIVE ILEUS ( 1 FDA reports)
PREGNANCY OF PARTNER ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SHOULDER ARTHROPLASTY ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL CORD OPERATION ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STOOLS WATERY ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TOXIC OPTIC NEUROPATHY ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)

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