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

DEPRESSION ( 25 FDA reports)
CONDITION AGGRAVATED ( 17 FDA reports)
DRUG INEFFECTIVE ( 15 FDA reports)
SUICIDE ATTEMPT ( 15 FDA reports)
INSOMNIA ( 13 FDA reports)
LOSS OF CONSCIOUSNESS ( 12 FDA reports)
ANXIETY ( 11 FDA reports)
CROHN'S DISEASE ( 10 FDA reports)
ERYTHEMA ( 10 FDA reports)
FALL ( 10 FDA reports)
DIZZINESS ( 9 FDA reports)
NAUSEA ( 9 FDA reports)
SOMNOLENCE ( 9 FDA reports)
AMNESIA ( 8 FDA reports)
DYSPNOEA ( 8 FDA reports)
HEADACHE ( 8 FDA reports)
HYPERTENSION ( 8 FDA reports)
WEIGHT INCREASED ( 8 FDA reports)
ABASIA ( 7 FDA reports)
CEREBROVASCULAR ACCIDENT ( 7 FDA reports)
FEELING ABNORMAL ( 7 FDA reports)
PARAESTHESIA ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
ARTHRALGIA ( 6 FDA reports)
ARTHRITIS ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
INTENTIONAL MISUSE ( 6 FDA reports)
INTENTIONAL OVERDOSE ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
PAIN ( 6 FDA reports)
VOMITING ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
COMA ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
DRUG EFFECT DECREASED ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
SLEEP DISORDER ( 5 FDA reports)
SUICIDAL IDEATION ( 5 FDA reports)
TREMOR ( 5 FDA reports)
ANGER ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BODY HEIGHT DECREASED ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
COORDINATION ABNORMAL ( 4 FDA reports)
DIFFICULTY IN WALKING ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
FEELING JITTERY ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HYDROCELE ( 4 FDA reports)
IMPULSE-CONTROL DISORDER ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
KNEE ARTHROPLASTY ( 4 FDA reports)
NERVOUSNESS ( 4 FDA reports)
NEURALGIA ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PNEUMONIA VIRAL ( 4 FDA reports)
SELF-MEDICATION ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
AGITATION ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BABESIOSIS ( 3 FDA reports)
BLADDER PROLAPSE ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
CRYING ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
FACIAL PALSY ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HEARING IMPAIRED ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LYME DISEASE ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
MUSCLE CRAMP ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
RASH ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
THINKING ABNORMAL ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BACK INJURY ( 2 FDA reports)
BLOOD OSMOLARITY INCREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CATHETER SEPSIS ( 2 FDA reports)
CHANGE OF BOWEL HABIT ( 2 FDA reports)
COLITIS COLLAGENOUS ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOMANIA ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUPUS-LIKE SYNDROME ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OESOPHAGEAL DISORDER ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 2 FDA reports)
PERITONEAL CYST ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SCROTAL OEDEMA ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALLERGY TO PLANTS ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD FOLATE ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTEROCUTANEOUS FISTULA ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEMALE GENITAL-DIGESTIVE TRACT FISTULA ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYDROCELE FEMALE ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJURY ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTESTINAL STOMA COMPLICATION ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIC ULCER ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEIOMYOSARCOMA ( 1 FDA reports)
LIGAMENT INJURY ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MASS ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PENIS DEVIATION ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHOBIA ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOMOTOR AGITATION ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SERUM SEROTONIN DECREASED ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBMANDIBULAR MASS ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TREMOR NEONATAL ( 1 FDA reports)
ULCER ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UTERINE LEIOMYOSARCOMA ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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