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

DRUG INEFFECTIVE ( 48 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 32 FDA reports)
FATIGUE ( 29 FDA reports)
COMPLETED SUICIDE ( 28 FDA reports)
NAUSEA ( 27 FDA reports)
HEADACHE ( 26 FDA reports)
ASTHENIA ( 25 FDA reports)
FEELING ABNORMAL ( 22 FDA reports)
PNEUMONIA ( 21 FDA reports)
ANXIETY ( 20 FDA reports)
FALL ( 20 FDA reports)
CHOLELITHIASIS ( 18 FDA reports)
INSOMNIA ( 18 FDA reports)
PAIN ( 18 FDA reports)
ABDOMINAL PAIN ( 16 FDA reports)
AGITATION ( 16 FDA reports)
DEPRESSION ( 16 FDA reports)
DYSPNOEA ( 16 FDA reports)
DEATH ( 15 FDA reports)
DIZZINESS ( 15 FDA reports)
CHOLECYSTITIS CHRONIC ( 14 FDA reports)
DISTURBANCE IN ATTENTION ( 14 FDA reports)
GALLBLADDER DISORDER ( 14 FDA reports)
PULMONARY EMBOLISM ( 14 FDA reports)
MALAISE ( 13 FDA reports)
PALPITATIONS ( 13 FDA reports)
SOMNOLENCE ( 13 FDA reports)
CHEST PAIN ( 12 FDA reports)
DIARRHOEA ( 12 FDA reports)
HYPERHIDROSIS ( 12 FDA reports)
SUICIDAL IDEATION ( 12 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 12 FDA reports)
BLOOD PRESSURE DECREASED ( 11 FDA reports)
CARDIAC ARREST ( 11 FDA reports)
DEEP VEIN THROMBOSIS ( 11 FDA reports)
DRUG INTERACTION ( 11 FDA reports)
IRRITABILITY ( 11 FDA reports)
LOSS OF CONSCIOUSNESS ( 11 FDA reports)
MEMORY IMPAIRMENT ( 11 FDA reports)
MULTIPLE SCLEROSIS ( 11 FDA reports)
ABDOMINAL PAIN UPPER ( 10 FDA reports)
CACHEXIA ( 10 FDA reports)
PULMONARY OEDEMA ( 10 FDA reports)
RESPIRATORY DISTRESS ( 10 FDA reports)
ABNORMAL BEHAVIOUR ( 9 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 9 FDA reports)
HAEMATOCHEZIA ( 9 FDA reports)
HEPATITIS C ( 9 FDA reports)
PRODUCT QUALITY ISSUE ( 9 FDA reports)
RESPIRATORY ARREST ( 9 FDA reports)
AGGRESSION ( 8 FDA reports)
CONFUSIONAL STATE ( 8 FDA reports)
CRYING ( 8 FDA reports)
DYSARTHRIA ( 8 FDA reports)
DYSPEPSIA ( 8 FDA reports)
HYPERBILIRUBINAEMIA ( 8 FDA reports)
INJURY ( 8 FDA reports)
MOOD SWINGS ( 8 FDA reports)
PLEURAL EFFUSION ( 8 FDA reports)
POISONING ( 8 FDA reports)
STAPHYLOCOCCAL INFECTION ( 8 FDA reports)
TREMOR ( 8 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
HYPOXIA ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
VOMITING ( 7 FDA reports)
ANGER ( 6 FDA reports)
CHOLECYSTITIS ( 6 FDA reports)
CHROMATURIA ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DRUG EFFECT DECREASED ( 6 FDA reports)
DRY MOUTH ( 6 FDA reports)
ENCEPHALOPATHY ( 6 FDA reports)
FAECES PALE ( 6 FDA reports)
HEART RATE INCREASED ( 6 FDA reports)
HEPATIC ENZYME INCREASED ( 6 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 6 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 6 FDA reports)
INTENTIONAL OVERDOSE ( 6 FDA reports)
JAUNDICE ( 6 FDA reports)
MENINGITIS BACTERIAL ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
PARAESTHESIA ( 6 FDA reports)
VENTRICULAR TACHYCARDIA ( 6 FDA reports)
WEIGHT DECREASED ( 6 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
BILIARY COLIC ( 5 FDA reports)
BIPOLAR DISORDER ( 5 FDA reports)
BLOOD CULTURE POSITIVE ( 5 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 5 FDA reports)
CHOLECYSTITIS ACUTE ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
DISORIENTATION ( 5 FDA reports)
DRUG DOSE OMISSION ( 5 FDA reports)
FLUID IMBALANCE ( 5 FDA reports)
HYDROCEPHALUS ( 5 FDA reports)
HYPERNATRAEMIA ( 5 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 5 FDA reports)
INCORRECT DOSE ADMINISTERED ( 5 FDA reports)
INTENTIONAL DRUG MISUSE ( 5 FDA reports)
MENTAL STATUS CHANGES ( 5 FDA reports)
NERVOUS SYSTEM DISORDER ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
SEDATION ( 5 FDA reports)
SOMNAMBULISM ( 5 FDA reports)
TENSION ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
WITHDRAWAL SYNDROME ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ARTHROPATHY ( 4 FDA reports)
ATELECTASIS ( 4 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CNS VENTRICULITIS ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
COUGH ( 4 FDA reports)
DRUG ABUSE ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
INJECTION SITE ERYTHEMA ( 4 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 4 FDA reports)
LOWER LIMB FRACTURE ( 4 FDA reports)
LYMPHADENOPATHY ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
PARANOIA ( 4 FDA reports)
PROCEDURAL PAIN ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
RASH ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
ROAD TRAFFIC ACCIDENT ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
STRESS ( 4 FDA reports)
VARICES OESOPHAGEAL ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD MAGNESIUM DECREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BLOOD SODIUM INCREASED ( 3 FDA reports)
CALCIUM IONISED DECREASED ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CRIME ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DRUG DIVERSION ( 3 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 3 FDA reports)
GALLBLADDER INJURY ( 3 FDA reports)
GALLBLADDER PAIN ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
IMPAIRED WORK ABILITY ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LIP INJURY ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
LOGORRHOEA ( 3 FDA reports)
MASTOIDITIS ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MYELITIS TRANSVERSE ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
NIGHT SWEATS ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
POSTURING ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SUBSTANCE ABUSE ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABSCESS INTESTINAL ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
AMPHETAMINES POSITIVE ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
APLASIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
BLOOD OSMOLARITY INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CATATONIA ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
DECREASED INTEREST ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DEPRESSIVE SYMPTOM ( 2 FDA reports)
DEVICE LEAKAGE ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG DETOXIFICATION ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FEAR ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GALLBLADDER POLYP ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HOMICIDE ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOAESTHESIA FACIAL ( 2 FDA reports)
HYPOMANIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
LIGAMENT INJURY ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
MICROCOCCUS INFECTION ( 2 FDA reports)
MOUTH INJURY ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEUTROPENIC INFECTION ( 2 FDA reports)
OBESITY ( 2 FDA reports)
ORAL DISCHARGE ( 2 FDA reports)
OVARIAN CYST RUPTURED ( 2 FDA reports)
PEAU D'ORANGE ( 2 FDA reports)
PERFORATION BILE DUCT ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 2 FDA reports)
PRODUCT FORMULATION ISSUE ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 2 FDA reports)
SEASONAL ALLERGY ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SYNOVIAL CYST ( 2 FDA reports)
TACHYPHRENIA ( 2 FDA reports)
TESTICULAR PAIN ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
TONGUE DRY ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
UTERINE RUPTURE ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
APATHY ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD HEAVY METAL INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CHANGE IN SUSTAINED ATTENTION ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLESTEROSIS ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DETOXIFICATION ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 1 FDA reports)
IUCD COMPLICATION ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NODULE ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREAS ISLET CELL TRANSPLANT ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POSTOPERATIVE ILEUS ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PRODUCT ODOUR ABNORMAL ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PROTEIN S DEFICIENCY ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PYROMANIA ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SLEEP-RELATED EATING DISORDER ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SPINAL COLUMN INJURY ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THIRST ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TOURETTE'S DISORDER ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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